rs1366906380 | p.Trp5Cys | missense variant | - | NC_000007.14:g.41700360C>A | gnomAD |
rs1164410355 | p.Gly8Glu | missense variant | - | NC_000007.14:g.41700352C>T | gnomAD |
rs1156510703 | p.Gly8Arg | missense variant | - | NC_000007.14:g.41700353C>T | TOPMed |
rs1429366494 | p.Phe9Leu | missense variant | - | NC_000007.14:g.41700348A>C | gnomAD |
NCI-TCGA novel | p.Ala12Thr | missense variant | - | NC_000007.14:g.41700341C>T | NCI-TCGA |
rs1488241309 | p.Ala12Ser | missense variant | - | NC_000007.14:g.41700341C>A | gnomAD |
rs777959895 | p.Cys14Tyr | missense variant | - | NC_000007.14:g.41700334C>T | ExAC,gnomAD |
rs777959895 | p.Cys14Phe | missense variant | - | NC_000007.14:g.41700334C>A | ExAC,gnomAD |
rs149209111 | p.Cys14Ser | missense variant | - | NC_000007.14:g.41700335A>T | ESP,TOPMed |
NCI-TCGA novel | p.Trp15Arg | missense variant | - | NC_000007.14:g.41700332A>T | NCI-TCGA |
rs933197708 | p.Trp15Cys | missense variant | - | NC_000007.14:g.41700330C>A | TOPMed |
rs758814874 | p.Ile16Thr | missense variant | - | NC_000007.14:g.41700328A>G | ExAC,gnomAD |
NCI-TCGA novel | p.Val18Leu | missense variant | - | NC_000007.14:g.41700323C>A | NCI-TCGA |
COSM3923617 | p.Ser21Phe | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700313G>A | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Thr23ProPheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41700309G>- | NCI-TCGA |
rs765780968 | p.Pro24Leu | missense variant | - | NC_000007.14:g.41700304G>A | ExAC,gnomAD |
rs1444327391 | p.Pro24Ala | missense variant | - | NC_000007.14:g.41700305G>C | TOPMed |
NCI-TCGA novel | p.Gly25Ter | stop gained | - | NC_000007.14:g.41700302C>A | NCI-TCGA |
rs755619740 | p.Ser26Phe | missense variant | - | NC_000007.14:g.41700298G>A | ExAC,TOPMed,gnomAD |
rs1372354341 | p.Glu27Gln | missense variant | - | NC_000007.14:g.41700296C>G | TOPMed |
rs972161023 | p.Gly28Glu | missense variant | - | NC_000007.14:g.41700292C>T | gnomAD |
NCI-TCGA novel | p.Gly28Arg | missense variant | - | NC_000007.14:g.41700293C>T | NCI-TCGA |
rs534590694 | p.His29Asp | missense variant | - | NC_000007.14:g.41700290G>C | 1000Genomes,ExAC,gnomAD |
rs534590694 | p.His29Tyr | missense variant | - | NC_000007.14:g.41700290G>A | 1000Genomes,ExAC,gnomAD |
COSM3638689 | p.Ser30Asn | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700286C>T | NCI-TCGA Cosmic |
rs942081109 | p.Ser30Arg | missense variant | - | NC_000007.14:g.41700285G>T | - |
rs1283898685 | p.Ala31Pro | missense variant | - | NC_000007.14:g.41700284C>G | gnomAD |
rs761497837 | p.Ala31Val | missense variant | - | NC_000007.14:g.41700283G>A | ExAC,TOPMed,gnomAD |
rs376838491 | p.Ala32Thr | missense variant | - | NC_000007.14:g.41700281C>T | ESP,ExAC,TOPMed,gnomAD |
rs1488136875 | p.Ala32Gly | missense variant | - | NC_000007.14:g.41700280G>C | gnomAD |
rs762816927 | p.Pro33Thr | missense variant | - | NC_000007.14:g.41700278G>T | ExAC,gnomAD |
rs1261664857 | p.Asp34Asn | missense variant | - | NC_000007.14:g.41700275C>T | gnomAD |
rs201591674 | p.Pro36Arg | missense variant | - | NC_000007.14:g.41700268G>C | ExAC,gnomAD |
COSM1089620 | p.Ala39Val | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700259G>A | NCI-TCGA Cosmic |
rs373520349 | p.Ala39Glu | missense variant | - | NC_000007.14:g.41700259G>T | ESP,ExAC,TOPMed,gnomAD |
rs1232597234 | p.Leu40Pro | missense variant | - | NC_000007.14:g.41700256A>G | TOPMed |
rs771248041 | p.Leu40Val | missense variant | - | NC_000007.14:g.41700257G>C | ExAC,gnomAD |
rs373322295 | p.Ala41Val | missense variant | - | NC_000007.14:g.41700253G>A | ESP,ExAC,TOPMed,gnomAD |
rs984438766 | p.Ala41Thr | missense variant | - | NC_000007.14:g.41700254C>T | TOPMed,gnomAD |
rs373322295 | p.Ala41Gly | missense variant | - | NC_000007.14:g.41700253G>C | ESP,ExAC,TOPMed,gnomAD |
rs376794102 | p.Ala42Thr | missense variant | - | NC_000007.14:g.41700251C>T | ExAC,gnomAD |
rs376794102 | p.Ala42Ser | missense variant | - | NC_000007.14:g.41700251C>A | ExAC,gnomAD |
rs953665038 | p.Lys45Arg | missense variant | - | NC_000007.14:g.41700241T>C | TOPMed,gnomAD |
rs1316814689 | p.Pro48Leu | missense variant | - | NC_000007.14:g.41700232G>A | TOPMed,gnomAD |
rs1316814689 | p.Pro48His | missense variant | - | NC_000007.14:g.41700232G>T | TOPMed,gnomAD |
rs1235277612 | p.Asn49Ser | missense variant | - | NC_000007.14:g.41700229T>C | gnomAD |
rs779271157 | p.Ser50Tyr | missense variant | - | NC_000007.14:g.41700226G>T | ExAC,gnomAD |
rs779271157 | p.Ser50Cys | missense variant | - | NC_000007.14:g.41700226G>C | ExAC,gnomAD |
COSM1450706 | p.Pro52Ser | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700221G>A | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Pro52Gln | missense variant | - | NC_000007.14:g.41700220G>T | NCI-TCGA |
rs1030538647 | p.Met54Ile | missense variant | - | NC_000007.14:g.41700213C>A | TOPMed |
NCI-TCGA novel | p.Glu56Asp | missense variant | - | NC_000007.14:g.41700207C>A | NCI-TCGA |
NCI-TCGA novel | p.Ala57Val | missense variant | - | NC_000007.14:g.41700205G>A | NCI-TCGA |
rs1329616704 | p.Val58Leu | missense variant | - | NC_000007.14:g.41700203C>G | gnomAD |
rs749899848 | p.His61Tyr | missense variant | - | NC_000007.14:g.41700194G>A | ExAC,gnomAD |
NCI-TCGA novel | p.Asn64Lys | missense variant | - | NC_000007.14:g.41700183G>C | NCI-TCGA |
rs1441973969 | p.Arg71Ser | missense variant | - | NC_000007.14:g.41700162T>G | gnomAD |
rs751118764 | p.Pro72His | missense variant | - | NC_000007.14:g.41700160G>T | ExAC,gnomAD |
rs762653354 | p.Asp73Asn | missense variant | - | NC_000007.14:g.41700158C>T | ExAC,gnomAD |
NCI-TCGA novel | p.Val74Ala | missense variant | - | NC_000007.14:g.41700154A>G | NCI-TCGA |
rs182017908 | p.Thr75Ser | missense variant | - | NC_000007.14:g.41700151G>C | 1000Genomes,ExAC,TOPMed,gnomAD |
rs752596382 | p.Thr75Pro | missense variant | - | NC_000007.14:g.41700152T>G | ExAC,gnomAD |
rs182017908 | p.Thr75Ile | missense variant | - | NC_000007.14:g.41700151G>A | 1000Genomes,ExAC,TOPMed,gnomAD |
rs776731486 | p.Gln76Ter | stop gained | - | NC_000007.14:g.41700149G>A | ExAC |
NCI-TCGA novel | p.Gln76His | missense variant | - | NC_000007.14:g.41700147C>A | NCI-TCGA |
NCI-TCGA novel | p.Pro77Ala | missense variant | - | NC_000007.14:g.41700146G>C | NCI-TCGA |
rs771076354 | p.Val78Ile | missense variant | - | NC_000007.14:g.41700143C>T | ExAC,TOPMed,gnomAD |
rs760840635 | p.Pro79Ser | missense variant | - | NC_000007.14:g.41700140G>A | ExAC,gnomAD |
NCI-TCGA novel | p.Pro79Leu | missense variant | - | NC_000007.14:g.41700139G>A | NCI-TCGA |
rs1339554915 | p.Lys80Thr | missense variant | - | NC_000007.14:g.41700136T>G | gnomAD |
COSM1089617 | p.Ala81Val | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700133G>A | NCI-TCGA Cosmic |
COSM6177881 | p.Ala81Glu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700133G>T | NCI-TCGA Cosmic |
COSM3880978 | p.Ala82Val | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700130G>A | NCI-TCGA Cosmic |
rs1446232934 | p.Ala82Thr | missense variant | - | NC_000007.14:g.41700131C>T | gnomAD |
rs748436551 | p.Leu83Val | missense variant | - | NC_000007.14:g.41700128G>C | ExAC,gnomAD |
rs779371975 | p.Asn85Ser | missense variant | - | NC_000007.14:g.41700121T>C | ExAC,TOPMed,gnomAD |
rs749750926 | p.Ala86Val | missense variant | - | NC_000007.14:g.41700118G>A | ExAC,gnomAD |
rs756693243 | p.Ile87Met | missense variant | - | NC_000007.14:g.41700114G>C | ExAC,gnomAD |
rs777279223 | p.His91Arg | missense variant | - | NC_000007.14:g.41700103T>C | ExAC,gnomAD |
rs752403730 | p.Val95Ile | missense variant | - | NC_000007.14:g.41700092C>T | ExAC,gnomAD |
rs540086083 | p.Glu97Gln | missense variant | - | NC_000007.14:g.41700086C>G | 1000Genomes,ExAC,gnomAD |
NCI-TCGA novel | p.Glu97Asp | missense variant | - | NC_000007.14:g.41700084C>A | NCI-TCGA |
rs149702280 | p.Asn98Lys | missense variant | - | NC_000007.14:g.41700081G>T | ESP,ExAC,TOPMed,gnomAD |
rs773386945 | p.Tyr100Asn | missense variant | - | NC_000007.14:g.41700077A>T | ExAC,gnomAD |
rs1476143414 | p.Asp105Tyr | missense variant | - | NC_000007.14:g.41700062C>A | TOPMed |
COSM1131585 | p.Ile107Asn | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700055A>T | NCI-TCGA Cosmic |
rs1001765662 | p.Ile107Ser | missense variant | - | NC_000007.14:g.41700055A>C | TOPMed |
rs1001765662 | p.Ile107Thr | missense variant | - | NC_000007.14:g.41700055A>G | TOPMed |
NCI-TCGA novel | p.Gly108Glu | missense variant | - | NC_000007.14:g.41700052C>T | NCI-TCGA |
rs551268437 | p.Gly108Arg | missense variant | - | NC_000007.14:g.41700053C>T | 1000Genomes,ExAC,gnomAD |
rs1339899817 | p.Ala111Glu | missense variant | - | NC_000007.14:g.41700043G>T | gnomAD |
NCI-TCGA novel | p.Glu112Ter | stop gained | - | NC_000007.14:g.41700041C>A | NCI-TCGA |
rs768954945 | p.Met113Val | missense variant | - | NC_000007.14:g.41700038T>C | ExAC,gnomAD |
COSM746913 | p.Glu115Gln | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700032C>G | NCI-TCGA Cosmic |
COSM1254835 | p.Leu116Pro | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700028A>G | NCI-TCGA Cosmic |
COSM1450705 | p.Leu116Arg | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700028A>C | NCI-TCGA Cosmic |
rs780538034 | p.Leu116Phe | missense variant | - | NC_000007.14:g.41700029G>A | ExAC,gnomAD |
rs777383877 | p.Met117Thr | missense variant | - | NC_000007.14:g.41700025A>G | ExAC,TOPMed,gnomAD |
rs746480596 | p.Met117Val | missense variant | - | NC_000007.14:g.41700026T>C | ExAC |
COSM3638688 | p.Glu118Lys | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41700023C>T | NCI-TCGA Cosmic |
rs747778899 | p.Gln119Glu | missense variant | - | NC_000007.14:g.41700020G>C | ExAC,gnomAD |
rs778711643 | p.Thr120Ile | missense variant | - | NC_000007.14:g.41700016G>A | ExAC,gnomAD |
NCI-TCGA novel | p.Glu122Asp | missense variant | - | NC_000007.14:g.41700009C>A | NCI-TCGA |
rs1261026870 | p.Glu128Gln | missense variant | - | NC_000007.14:g.41699993C>G | gnomAD |
NCI-TCGA novel | p.Gly130Arg | missense variant | - | NC_000007.14:g.41699987C>T | NCI-TCGA |
rs764280388 | p.Thr131Ile | missense variant | - | NC_000007.14:g.41690539G>A | ExAC,TOPMed,gnomAD |
rs1369747479 | p.Ala132Asp | missense variant | - | NC_000007.14:g.41690536G>T | TOPMed,gnomAD |
rs763203259 | p.Arg133Lys | missense variant | - | NC_000007.14:g.41690533C>T | ExAC,gnomAD |
rs765588441 | p.Lys134Glu | missense variant | - | NC_000007.14:g.41690531T>C | ExAC,TOPMed,gnomAD |
rs142519810 | p.Thr135Met | missense variant | - | NC_000007.14:g.41690527G>A | ESP,ExAC,TOPMed,gnomAD |
COSM6177882 | p.Glu139Asp | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690514C>G | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Glu139Lys | missense variant | - | NC_000007.14:g.41690516C>T | NCI-TCGA |
rs139371691 | p.Glu139Ala | missense variant | - | NC_000007.14:g.41690515T>G | ESP,ExAC,TOPMed,gnomAD |
COSM4820280 | p.Ile140Thr | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690512A>G | NCI-TCGA Cosmic |
COSM3638685 | p.Ser141Phe | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690509G>A | NCI-TCGA Cosmic |
COSM6177883 | p.Lys142Asn | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690505C>A | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Glu143Lys | missense variant | - | NC_000007.14:g.41690504C>T | NCI-TCGA |
rs1221555253 | p.Glu143Ala | missense variant | - | NC_000007.14:g.41690503T>G | TOPMed |
NCI-TCGA novel | p.Gly144Asp | missense variant | - | NC_000007.14:g.41690500C>T | NCI-TCGA |
rs979257752 | p.Asp146Asn | missense variant | - | NC_000007.14:g.41690495C>T | gnomAD |
NCI-TCGA novel | p.Glu151Gln | missense variant | - | NC_000007.14:g.41690480C>G | NCI-TCGA |
rs377167564 | p.Arg152His | missense variant | - | NC_000007.14:g.41690476C>T | ESP,ExAC,TOPMed,gnomAD |
rs748897120 | p.Arg152Cys | missense variant | - | NC_000007.14:g.41690477G>A | ExAC,gnomAD |
rs377167564 | p.Arg152Leu | missense variant | - | NC_000007.14:g.41690476C>A | ESP,ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Glu154Lys | missense variant | - | NC_000007.14:g.41690471C>T | NCI-TCGA |
COSM1089616 | p.Trp156Ter | stop gained | Variant assessed as Somatic; HIGH impact. | NC_000007.14:g.41690464C>T | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Trp156Ter | stop gained | - | NC_000007.14:g.41690463C>T | NCI-TCGA |
rs769570431 | p.Leu159Val | missense variant | - | NC_000007.14:g.41690456G>C | ExAC,gnomAD |
NCI-TCGA novel | p.Val161SerPheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41690451T>- | NCI-TCGA |
rs1354806996 | p.Val161Phe | missense variant | - | NC_000007.14:g.41690450C>A | gnomAD |
COSM3638684 | p.Pro162Ser | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690447G>A | NCI-TCGA Cosmic |
COSM3880976 | p.Pro162His | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690446G>T | NCI-TCGA Cosmic |
rs1397640362 | p.Pro162Leu | missense variant | - | NC_000007.14:g.41690446G>A | gnomAD |
rs373733975 | p.Ala164Thr | missense variant | - | NC_000007.14:g.41690441C>T | ESP,ExAC,gnomAD |
rs1374218408 | p.Arg166Ser | missense variant | - | NC_000007.14:g.41690433C>A | TOPMed,gnomAD |
rs781179854 | p.Arg166Trp | missense variant | - | NC_000007.14:g.41690435T>A | ExAC,gnomAD |
COSM3638683 | p.Arg168Lys | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690428C>T | NCI-TCGA Cosmic |
rs777791358 | p.Lys170Ile | missense variant | - | NC_000007.14:g.41690422T>A | ExAC,TOPMed,gnomAD |
rs777791358 | p.Lys170Thr | missense variant | - | NC_000007.14:g.41690422T>G | ExAC,TOPMed,gnomAD |
rs1434057860 | p.Val171Ile | missense variant | - | NC_000007.14:g.41690420C>T | gnomAD |
COSM601369 | p.Arg174Ser | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690411G>T | NCI-TCGA Cosmic |
rs537531066 | p.Arg174His | missense variant | - | NC_000007.14:g.41690410C>T | 1000Genomes,ExAC,TOPMed,gnomAD |
rs758496316 | p.Arg174Cys | missense variant | - | NC_000007.14:g.41690411G>A | ExAC,gnomAD |
rs537531066 | p.Arg174Leu | missense variant | - | NC_000007.14:g.41690410C>A | 1000Genomes,ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Leu175SerPheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41690408G>- | NCI-TCGA |
rs1182490702 | p.Phe176Ile | missense variant | - | NC_000007.14:g.41690405A>T | gnomAD |
COSM6110269 | p.Gln177Glu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690402G>C | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Gln177His | missense variant | - | NC_000007.14:g.41690400C>G | NCI-TCGA |
rs759930790 | p.Gln178Arg | missense variant | - | NC_000007.14:g.41690398T>C | ExAC,gnomAD |
COSM5768309 | p.Gln179Ter | stop gained | Variant assessed as Somatic; HIGH impact. | NC_000007.14:g.41690396G>A | NCI-TCGA Cosmic |
rs766876018 | p.Gln179Pro | missense variant | - | NC_000007.14:g.41690395T>G | ExAC,gnomAD |
rs761221455 | p.Gln179His | missense variant | - | NC_000007.14:g.41690394C>A | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Gln179Glu | missense variant | - | NC_000007.14:g.41690396G>C | NCI-TCGA |
COSM3431597 | p.Pro182Leu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690386G>A | NCI-TCGA Cosmic |
rs766987359 | p.Pro182Gln | missense variant | - | NC_000007.14:g.41690386G>T | ExAC,TOPMed,gnomAD |
rs766987359 | p.Pro182Arg | missense variant | - | NC_000007.14:g.41690386G>C | ExAC,TOPMed,gnomAD |
rs773874254 | p.Pro182Ala | missense variant | - | NC_000007.14:g.41690387G>C | ExAC,gnomAD |
rs769393297 | p.Gly184Ser | missense variant | - | NC_000007.14:g.41690381C>T | ExAC,gnomAD |
rs868188277 | p.Ser185Asn | missense variant | - | NC_000007.14:g.41690377C>T | gnomAD |
rs868188277 | p.Ser185Thr | missense variant | - | NC_000007.14:g.41690377C>G | gnomAD |
COSM3638682 | p.Asp187Asn | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690372C>T | NCI-TCGA Cosmic |
rs1380653684 | p.Asp187His | missense variant | - | NC_000007.14:g.41690372C>G | TOPMed,gnomAD |
rs1025790050 | p.Gly189Arg | missense variant | - | NC_000007.14:g.41690366C>T | TOPMed,gnomAD |
rs867739441 | p.Glu190Lys | missense variant | - | NC_000007.14:g.41690363C>T | - |
NCI-TCGA novel | p.Glu190Ter | stop gained | - | NC_000007.14:g.41690363C>A | NCI-TCGA |
NCI-TCGA novel | p.Glu190GlnPheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41690363_41690364insCCCTGTGTCCAAGCTG | NCI-TCGA |
NCI-TCGA novel | p.Glu191Lys | missense variant | - | NC_000007.14:g.41690360C>T | NCI-TCGA |
rs138705117 | p.Glu191Asp | missense variant | - | NC_000007.14:g.41690358C>G | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs780890864 | p.Ala192Ser | missense variant | - | NC_000007.14:g.41690357C>A | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Ala192Val | missense variant | - | NC_000007.14:g.41690356G>A | NCI-TCGA |
rs780890864 | p.Ala192Thr | missense variant | - | NC_000007.14:g.41690357C>T | ExAC,TOPMed,gnomAD |
rs1007889051 | p.Glu193Lys | missense variant | - | NC_000007.14:g.41690354C>T | TOPMed,gnomAD |
rs1165688714 | p.Glu194Gln | missense variant | - | NC_000007.14:g.41690351C>G | gnomAD |
rs1165688714 | p.Glu194Lys | missense variant | - | NC_000007.14:g.41690351C>T | gnomAD |
rs746900962 | p.Val195Glu | missense variant | - | NC_000007.14:g.41690347A>T | ExAC |
rs200425294 | p.Gly196Asp | missense variant | - | NC_000007.14:g.41690344C>T | ExAC,TOPMed,gnomAD |
rs1425813756 | p.Gly196Ser | missense variant | - | NC_000007.14:g.41690345C>T | gnomAD |
rs1345043414 | p.Lys198Met | missense variant | - | NC_000007.14:g.41690338T>A | TOPMed |
rs111379520 | p.Gly199Glu | missense variant | - | NC_000007.14:g.41690335C>T | ExAC,TOPMed,gnomAD |
rs146325702 | p.Gly199Arg | missense variant | - | NC_000007.14:g.41690336C>T | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs146325702 | p.Gly199Trp | missense variant | - | NC_000007.14:g.41690336C>A | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs146325702 | p.Gly199Arg | missense variant | - | NC_000007.14:g.41690336C>G | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs111379520 | p.Gly199Ala | missense variant | - | NC_000007.14:g.41690335C>G | ExAC,TOPMed,gnomAD |
rs1379000367 | p.Glu200Lys | missense variant | - | NC_000007.14:g.41690333C>T | gnomAD |
rs1214870637 | p.Arg201Lys | missense variant | - | NC_000007.14:g.41690329C>T | gnomAD |
COSM3412043 | p.Ser202Cys | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690327T>A | NCI-TCGA Cosmic |
COSM4921135 | p.Glu203Ter | stop gained | Variant assessed as Somatic; HIGH impact. | NC_000007.14:g.41690324C>A | NCI-TCGA Cosmic |
COSM3923616 | p.Glu203Lys | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690324C>T | NCI-TCGA Cosmic |
rs376470270 | p.Leu204Arg | missense variant | - | NC_000007.14:g.41690320A>C | ESP |
NCI-TCGA novel | p.Leu204Met | missense variant | - | NC_000007.14:g.41690321G>T | NCI-TCGA |
rs1266432565 | p.Leu206Val | missense variant | - | NC_000007.14:g.41690315G>C | gnomAD |
rs1221757242 | p.del209TerSerTrpArgSerValGlyAlaHisArgValAlaGlnPro | stop gained | - | NC_000007.14:g.41690306_41690307insGGGCTGGGCAACTCTATGAGCACCCACACTCCTCCACGATCA | gnomAD |
rs1309932151 | p.Val210Leu | missense variant | - | NC_000007.14:g.41690303C>A | gnomAD |
COSM746914 | p.Val211Leu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690300C>A | NCI-TCGA Cosmic |
rs1309408013 | p.Val211Ile | missense variant | - | NC_000007.14:g.41690300C>T | gnomAD |
rs149369067 | p.Asp212Glu | missense variant | - | NC_000007.14:g.41690295G>T | ESP,ExAC,TOPMed,gnomAD |
rs762543780 | p.Ala213Thr | missense variant | - | NC_000007.14:g.41690294C>T | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Ala213Pro | missense variant | - | NC_000007.14:g.41690294C>G | NCI-TCGA |
NCI-TCGA novel | p.Ala213Val | missense variant | - | NC_000007.14:g.41690293G>A | NCI-TCGA |
rs762543780 | p.Ala213Ser | missense variant | - | NC_000007.14:g.41690294C>A | ExAC,TOPMed,gnomAD |
rs923669088 | p.Arg214Trp | missense variant | - | NC_000007.14:g.41690291G>A | - |
rs1043609570 | p.Arg214Gln | missense variant | - | NC_000007.14:g.41690290C>T | gnomAD |
NCI-TCGA novel | p.Lys215Glu | missense variant | - | NC_000007.14:g.41690288T>C | NCI-TCGA |
rs759072574 | p.Thr217Ser | missense variant | - | NC_000007.14:g.41690281G>C | ExAC,gnomAD |
NCI-TCGA novel | p.Thr217Ile | missense variant | - | NC_000007.14:g.41690281G>A | NCI-TCGA |
COSM1089615 | p.Trp218Ter | stop gained | Variant assessed as Somatic; HIGH impact. | NC_000007.14:g.41690277C>T | NCI-TCGA Cosmic |
rs776370904 | p.Phe221Leu | missense variant | - | NC_000007.14:g.41690268G>C | ExAC,gnomAD |
rs770655825 | p.Pro222Ser | missense variant | - | NC_000007.14:g.41690267G>A | ExAC,gnomAD |
rs138819536 | p.Arg229Pro | missense variant | - | NC_000007.14:g.41690245C>G | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs138819536 | p.Arg229Gln | missense variant | - | NC_000007.14:g.41690245C>T | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs908163566 | p.Arg229Trp | missense variant | - | NC_000007.14:g.41690246G>A | TOPMed |
rs1489240461 | p.Leu230Met | missense variant | - | NC_000007.14:g.41690243A>T | gnomAD |
rs748226962 | p.Leu231Met | missense variant | - | NC_000007.14:g.41690240G>T | ExAC,TOPMed,gnomAD |
rs980571220 | p.Gln233Glu | missense variant | - | NC_000007.14:g.41690234G>C | TOPMed,gnomAD |
NCI-TCGA novel | p.Gln233Ter | stop gained | - | NC_000007.14:g.41690234G>A | NCI-TCGA |
rs778816816 | p.Ser236Gly | missense variant | - | NC_000007.14:g.41690225T>C | ExAC,gnomAD |
rs1229001644 | p.Val240Phe | missense variant | - | NC_000007.14:g.41690213C>A | TOPMed |
rs1229001644 | p.Val240Ile | missense variant | - | NC_000007.14:g.41690213C>T | TOPMed |
rs150182559 | p.Arg241Trp | missense variant | - | NC_000007.14:g.41690210G>A | ESP,ExAC,TOPMed,gnomAD |
rs756546726 | p.Arg241Gln | missense variant | - | NC_000007.14:g.41690209C>T | ExAC,gnomAD |
COSM6110271 | p.Cys244Tyr | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690200C>T | NCI-TCGA Cosmic |
rs1365746909 | p.Glu245Lys | missense variant | - | NC_000007.14:g.41690198C>T | TOPMed,gnomAD |
rs1365746909 | p.Glu245Gln | missense variant | - | NC_000007.14:g.41690198C>G | TOPMed,gnomAD |
COSM6177885 | p.Gln246Leu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690194T>A | NCI-TCGA Cosmic |
rs757882910 | p.Gln246His | missense variant | - | NC_000007.14:g.41690193C>G | ExAC,gnomAD |
rs752140467 | p.Gln248Arg | missense variant | - | NC_000007.14:g.41690188T>C | ExAC,gnomAD |
rs764604932 | p.Ser250Asn | missense variant | - | NC_000007.14:g.41690182C>T | ExAC,gnomAD |
rs1168655188 | p.Gly251Cys | missense variant | - | NC_000007.14:g.41690180C>A | gnomAD |
COSM1089613 | p.Ala252Thr | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690177C>T | NCI-TCGA Cosmic |
rs1378762087 | p.Ala252Ser | missense variant | - | NC_000007.14:g.41690177C>A | gnomAD |
rs1290822028 | p.Ala252Asp | missense variant | - | NC_000007.14:g.41690176G>T | TOPMed |
rs1163090037 | p.Val255Phe | missense variant | - | NC_000007.14:g.41690168C>A | gnomAD |
NCI-TCGA novel | p.Val255Gly | missense variant | - | NC_000007.14:g.41690167A>C | NCI-TCGA |
COSM3638675 | p.Leu256Phe | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690165G>A | NCI-TCGA Cosmic |
rs1192011470 | p.Leu257Pro | missense variant | - | NC_000007.14:g.41690161A>G | TOPMed |
COSM1450702 | p.Gly258Arg | insertion | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690155_41690156insTCC | NCI-TCGA Cosmic |
rs1431859332 | p.Gly258Val | missense variant | - | NC_000007.14:g.41690158C>A | TOPMed,gnomAD |
rs1431859332 | p.Gly258Asp | missense variant | - | NC_000007.14:g.41690158C>T | TOPMed,gnomAD |
rs1178685586 | p.Gly258Ser | missense variant | - | NC_000007.14:g.41690159C>T | gnomAD |
rs1450176512 | p.Lys259Glu | missense variant | - | NC_000007.14:g.41690156T>C | TOPMed |
NCI-TCGA novel | p.Lys261Asn | missense variant | - | NC_000007.14:g.41690148C>G | NCI-TCGA |
NCI-TCGA novel | p.Lys262Met | missense variant | - | NC_000007.14:g.41690146T>A | NCI-TCGA |
COSM281930 | p.Glu264Ter | stop gained | Variant assessed as Somatic; HIGH impact. | NC_000007.14:g.41690141C>A | NCI-TCGA Cosmic |
rs1371913954 | p.Glu265Lys | missense variant | - | NC_000007.14:g.41690138C>T | TOPMed |
rs1192544869 | p.Glu265Gly | missense variant | - | NC_000007.14:g.41690137T>C | gnomAD |
COSM6110272 | p.Gly267Trp | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690132C>A | NCI-TCGA Cosmic |
rs760441012 | p.Gly267Arg | missense variant | - | NC_000007.14:g.41690132C>T | ExAC,gnomAD |
NCI-TCGA novel | p.Gly267Val | missense variant | - | NC_000007.14:g.41690131C>A | NCI-TCGA |
rs1193620503 | p.Gly267Ala | missense variant | - | NC_000007.14:g.41690131C>G | gnomAD |
NCI-TCGA novel | p.Glu268LysPheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41690129C>- | NCI-TCGA |
rs779220866 | p.Gly269Glu | missense variant | - | NC_000007.14:g.41690125C>T | TOPMed,gnomAD |
rs779220866 | p.Gly269Val | missense variant | - | NC_000007.14:g.41690125C>A | TOPMed,gnomAD |
rs771884298 | p.Lys271Arg | missense variant | - | NC_000007.14:g.41690119T>C | ExAC,TOPMed,gnomAD |
rs1390115330 | p.Lys272Arg | missense variant | - | NC_000007.14:g.41690116T>C | TOPMed |
NCI-TCGA novel | p.Gly273AlaPheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41690113C>- | NCI-TCGA |
rs1435204559 | p.Gly273Ser | missense variant | - | NC_000007.14:g.41690114C>T | TOPMed |
COSM321011 | p.Gly274Val | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690110C>A | NCI-TCGA Cosmic |
rs569482596 | p.Gly274Glu | missense variant | - | NC_000007.14:g.41690110C>T | 1000Genomes,ExAC,TOPMed,gnomAD |
rs768547360 | p.Gly274Arg | missense variant | - | NC_000007.14:g.41690111C>T | ExAC,TOPMed,gnomAD |
rs780414158 | p.Gly275Ser | missense variant | - | NC_000007.14:g.41690108C>T | ExAC,gnomAD |
rs1355421314 | p.Glu276Lys | missense variant | - | NC_000007.14:g.41690105C>T | TOPMed |
rs1390964419 | p.Gly277Ser | missense variant | - | NC_000007.14:g.41690102C>T | gnomAD |
rs1191953816 | p.Gly278Glu | missense variant | - | NC_000007.14:g.41690098C>T | gnomAD |
COSM485325 | p.Ala279Ser | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690096C>A | NCI-TCGA Cosmic |
rs1211988783 | p.Ala279Val | missense variant | - | NC_000007.14:g.41690095G>A | TOPMed |
rs951492435 | p.Gly280Arg | missense variant | - | NC_000007.14:g.41690093C>T | TOPMed,gnomAD |
VAR_072640 | p.Gly280Glu | Missense | - | - | UniProt |
rs1208258694 | p.Asp282Asn | missense variant | - | NC_000007.14:g.41690087C>T | TOPMed |
NCI-TCGA novel | p.Asp282Gly | missense variant | - | NC_000007.14:g.41690086T>C | NCI-TCGA |
COSM6177887 | p.Glu283Asp | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690082C>A | NCI-TCGA Cosmic |
rs1305050306 | p.Glu283Gln | missense variant | - | NC_000007.14:g.41690084C>G | gnomAD |
rs1488698571 | p.Glu284Lys | missense variant | - | NC_000007.14:g.41690081C>T | gnomAD |
rs1464988141 | p.Gln287Glu | missense variant | - | NC_000007.14:g.41690072G>C | gnomAD |
rs1159649174 | p.Pro291Ser | missense variant | - | NC_000007.14:g.41690060G>A | gnomAD |
rs1381819254 | p.Met294Thr | missense variant | - | NC_000007.14:g.41690050A>G | gnomAD |
NCI-TCGA novel | p.Met294Ile | missense variant | - | NC_000007.14:g.41690049C>A | NCI-TCGA |
COSM1329828 | p.Gln296His | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690043C>A | NCI-TCGA Cosmic |
COSM4692500 | p.Arg298Gln | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690038C>T | NCI-TCGA Cosmic |
rs373613637 | p.Arg298Trp | missense variant | - | NC_000007.14:g.41690039G>A | ESP,ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.His303Asn | missense variant | - | NC_000007.14:g.41690024G>T | NCI-TCGA |
rs564878978 | p.Arg306Gly | missense variant | - | NC_000007.14:g.41690015G>C | 1000Genomes,ExAC,gnomAD |
rs564878978 | p.Arg306Cys | missense variant | - | NC_000007.14:g.41690015G>A | 1000Genomes,ExAC,gnomAD |
rs1202073030 | p.Arg306His | missense variant | - | NC_000007.14:g.41690014C>T | gnomAD |
rs1202073030 | p.Arg306Pro | missense variant | - | NC_000007.14:g.41690014C>G | gnomAD |
rs564878978 | p.Arg306Ser | missense variant | - | NC_000007.14:g.41690015G>T | 1000Genomes,ExAC,gnomAD |
COSM1450701 | p.Arg308Cys | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690009G>A | NCI-TCGA Cosmic |
COSM6177888 | p.Arg309Leu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690005C>A | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Arg309Gln | missense variant | - | NC_000007.14:g.41690005C>T | NCI-TCGA |
COSM1089612 | p.Arg310Trp | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41690003G>A | NCI-TCGA Cosmic |
COSM3638671 | p.Gly311Asp | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689999C>T | NCI-TCGA Cosmic |
rs35168740 | p.Gly311Arg | missense variant | - | NC_000007.14:g.41690000C>G | TOPMed |
rs35168740 | p.Gly311Ser | missense variant | - | NC_000007.14:g.41690000C>T | TOPMed |
rs772872634 | p.Val318Ile | missense variant | - | NC_000007.14:g.41689979C>T | ExAC,gnomAD |
rs962913455 | p.Ile320Val | missense variant | - | NC_000007.14:g.41689973T>C | TOPMed,gnomAD |
rs1356119994 | p.Phe326Leu | missense variant | - | NC_000007.14:g.41689953G>T | TOPMed,gnomAD |
NCI-TCGA novel | p.Phe330Leu | missense variant | - | NC_000007.14:g.41689941G>T | NCI-TCGA |
rs138538132 | p.Gly334Ser | missense variant | - | NC_000007.14:g.41689931C>T | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs138538132 | p.Gly334Cys | missense variant | - | NC_000007.14:g.41689931C>A | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Gly334Asp | missense variant | - | NC_000007.14:g.41689930C>T | NCI-TCGA |
rs768700046 | p.Asn336Asp | missense variant | - | NC_000007.14:g.41689925T>C | ExAC,gnomAD |
rs762923659 | p.Asn336Lys | missense variant | - | NC_000007.14:g.41689923A>T | ExAC,gnomAD |
NCI-TCGA novel | p.Trp338Ter | stop gained | - | NC_000007.14:g.41689918C>T | NCI-TCGA |
NCI-TCGA novel | p.Trp338Arg | missense variant | - | NC_000007.14:g.41689919A>T | NCI-TCGA |
rs775755149 | p.Ile339Val | missense variant | - | NC_000007.14:g.41689916T>C | ExAC,gnomAD |
COSM746916 | p.Ala341Thr | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689910C>T | NCI-TCGA Cosmic |
COSM3638670 | p.Pro342Leu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689906G>A | NCI-TCGA Cosmic |
rs1238388233 | p.Ser343Cys | missense variant | - | NC_000007.14:g.41689903G>C | TOPMed |
rs1156386837 | p.Tyr345Cys | missense variant | - | NC_000007.14:g.41689897T>C | gnomAD |
NCI-TCGA novel | p.Ala347Val | missense variant | - | NC_000007.14:g.41689891G>A | NCI-TCGA |
rs771134702 | p.Asn348Ser | missense variant | - | NC_000007.14:g.41689888T>C | ExAC,gnomAD |
COSM298102 | p.Cys350Arg | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689883A>G | NCI-TCGA Cosmic |
RCV000709850 | p.Cys350Trp | missense variant | - | NC_000007.14:g.41689881G>C | ClinVar |
rs747474916 | p.Pro355Arg | missense variant | - | NC_000007.14:g.41689867G>C | ExAC,gnomAD |
rs747474916 | p.Pro355Leu | missense variant | - | NC_000007.14:g.41689867G>A | ExAC,gnomAD |
NCI-TCGA novel | p.Pro355Thr | missense variant | - | NC_000007.14:g.41689868G>T | NCI-TCGA |
NCI-TCGA novel | p.Ser356Cys | missense variant | - | NC_000007.14:g.41689865T>A | NCI-TCGA |
NCI-TCGA novel | p.Ser356Asn | missense variant | - | NC_000007.14:g.41689864C>T | NCI-TCGA |
NCI-TCGA novel | p.Ser362Phe | missense variant | - | NC_000007.14:g.41689846G>A | NCI-TCGA |
rs753232360 | p.Ser364Thr | missense variant | - | NC_000007.14:g.41689841A>T | ExAC,gnomAD |
NCI-TCGA novel | p.Ser364ProPheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41689842C>- | NCI-TCGA |
COSM5510214 | p.Ser370Leu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689822G>A | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Ser370Ter | stop gained | - | NC_000007.14:g.41689822G>C | NCI-TCGA |
rs1357347047 | p.Thr371Ile | missense variant | - | NC_000007.14:g.41689819G>A | gnomAD |
COSM6110273 | p.Val372Phe | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689817C>A | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Ile373Met | missense variant | - | NC_000007.14:g.41689812G>C | NCI-TCGA |
rs751423099 | p.Tyr376His | missense variant | - | NC_000007.14:g.41689805A>G | ExAC,gnomAD |
COSM1450700 | p.Arg377Cys | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689802G>A | NCI-TCGA Cosmic |
COSM188210 | p.Arg377His | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689801C>T | NCI-TCGA Cosmic |
COSM3229806 | p.Arg379Gln | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689795C>T | NCI-TCGA Cosmic |
COSM188209 | p.Arg379Trp | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689796G>A | NCI-TCGA Cosmic |
rs1361746138 | p.His381Arg | missense variant | - | NC_000007.14:g.41689789T>C | gnomAD |
NCI-TCGA novel | p.His381Asn | missense variant | - | NC_000007.14:g.41689790G>T | NCI-TCGA |
NCI-TCGA novel | p.His381IlePheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41689790G>- | NCI-TCGA |
NCI-TCGA novel | p.Ser382AlaPheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41689787T>- | NCI-TCGA |
rs376722349 | p.Ser382Arg | missense variant | - | NC_000007.14:g.41689785G>C | ESP,ExAC,TOPMed,gnomAD |
rs1157959739 | p.Pro383Leu | missense variant | - | NC_000007.14:g.41689783G>A | TOPMed |
rs1318105737 | p.Pro383Thr | missense variant | - | NC_000007.14:g.41689784G>T | gnomAD |
COSM1450697 | p.Ala385Ser | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689778C>A | NCI-TCGA Cosmic |
rs1399739221 | p.Asn386Lys | missense variant | - | NC_000007.14:g.41689773G>T | gnomAD |
rs1361491625 | p.Asn386Ser | missense variant | - | NC_000007.14:g.41689774T>C | TOPMed |
rs759695534 | p.Lys388Arg | missense variant | - | NC_000007.14:g.41689768T>C | ExAC,gnomAD |
NCI-TCGA novel | p.Ser389IlePheSerTerUnkUnk | frameshift | - | NC_000007.14:g.41689766_41689767insT | NCI-TCGA |
NCI-TCGA novel | p.Thr394Ser | missense variant | - | NC_000007.14:g.41689751T>A | NCI-TCGA |
rs771243659 | p.Lys395Arg | missense variant | - | NC_000007.14:g.41689747T>C | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Arg397Lys | missense variant | - | NC_000007.14:g.41689741C>T | NCI-TCGA |
rs747304324 | p.Pro398Ser | missense variant | - | NC_000007.14:g.41689739G>A | ExAC,gnomAD |
NCI-TCGA novel | p.Ser400Pro | missense variant | - | NC_000007.14:g.41689733A>G | NCI-TCGA |
COSM746917 | p.Asp405Asn | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689718C>T | NCI-TCGA Cosmic |
rs1374850253 | p.Asp406Ala | missense variant | - | NC_000007.14:g.41689714T>G | TOPMed |
rs772344962 | p.Gly407Cys | missense variant | - | NC_000007.14:g.41689712C>A | ExAC,TOPMed,gnomAD |
rs772344962 | p.Gly407Ser | missense variant | - | NC_000007.14:g.41689712C>T | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Lys412Arg | missense variant | - | NC_000007.14:g.41689696T>C | NCI-TCGA |
NCI-TCGA novel | p.Asp414His | missense variant | - | NC_000007.14:g.41689691C>G | NCI-TCGA |
rs779393124 | p.Asp414Tyr | missense variant | - | NC_000007.14:g.41689691C>A | ExAC,gnomAD |
COSM3880972 | p.Asn417Ser | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689681T>C | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Asn417His | missense variant | - | NC_000007.14:g.41689682T>G | NCI-TCGA |
NCI-TCGA novel | p.Met418Leu | missense variant | - | NC_000007.14:g.41689679T>A | NCI-TCGA |
rs749989847 | p.Val420Met | missense variant | - | NC_000007.14:g.41689673C>T | ExAC,gnomAD |
COSM3923615 | p.Glu421Lys | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689670C>T | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Gly424Val | missense variant | - | NC_000007.14:g.41689660C>A | NCI-TCGA |
NCI-TCGA novel | p.Cys425Tyr | missense variant | - | NC_000007.14:g.41689657C>T | NCI-TCGA |
COSM4807994 | p.Ser426Thr | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000007.14:g.41689655A>T | NCI-TCGA Cosmic |