COSM4404621 | p.Ser5Gly | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117622881A>G | NCI-TCGA Cosmic |
rs1443775776 | p.Ser5Asn | missense variant | - | NC_000001.11:g.117622882G>A | gnomAD |
rs1236957064 | p.Arg9Ser | missense variant | - | NC_000001.11:g.117622895G>C | TOPMed |
COSM3471991 | p.Asp10Asn | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117622896G>A | NCI-TCGA Cosmic |
rs772416638 | p.Cys11Arg | missense variant | - | NC_000001.11:g.117622899T>C | ExAC,TOPMed,gnomAD |
rs1324426912 | p.Met12Leu | missense variant | - | NC_000001.11:g.117622902A>C | TOPMed |
NCI-TCGA novel | p.Met12Val | missense variant | - | NC_000001.11:g.117622902A>G | NCI-TCGA |
rs773475817 | p.Met12Ile | missense variant | - | NC_000001.11:g.117622904G>T | ExAC,gnomAD |
rs34495780 | p.Val16Met | missense variant | - | NC_000001.11:g.117622914G>A | ESP,ExAC,TOPMed,gnomAD |
RCV000120905 | p.Val16Met | missense variant | - | NC_000001.11:g.117622914G>A | ClinVar |
rs1376138887 | p.Val16Gly | missense variant | - | NC_000001.11:g.117622915T>G | gnomAD |
rs776635415 | p.Asn18Ile | missense variant | - | NC_000001.11:g.117622921A>T | ExAC,gnomAD |
rs776635415 | p.Asn18Ser | missense variant | - | NC_000001.11:g.117622921A>G | ExAC,gnomAD |
rs912269955 | p.Asp20Tyr | missense variant | - | NC_000001.11:g.117622926G>T | TOPMed,gnomAD |
rs912269955 | p.Asp20Asn | missense variant | - | NC_000001.11:g.117622926G>A | TOPMed,gnomAD |
rs1279927757 | p.Gln21His | missense variant | - | NC_000001.11:g.117622931G>C | TOPMed |
rs1374365686 | p.Val28Ile | missense variant | - | NC_000001.11:g.117622950G>A | TOPMed |
RCV000120904 | p.Thr30Ser | missense variant | - | NC_000001.11:g.117622957C>G | ClinVar |
rs758089123 | p.Thr30Ala | missense variant | - | NC_000001.11:g.117622956A>G | ExAC,TOPMed,gnomAD |
rs758089123 | p.Thr30Ser | missense variant | - | NC_000001.11:g.117622956A>T | ExAC,TOPMed,gnomAD |
rs587778307 | p.Thr30Ser | missense variant | - | NC_000001.11:g.117622957C>G | - |
rs1260403191 | p.Val32Ile | missense variant | - | NC_000001.11:g.117622962G>A | gnomAD |
rs751161016 | p.Val33Ile | missense variant | - | NC_000001.11:g.117622965G>A | ExAC,gnomAD |
rs749814000 | p.Ile35Thr | missense variant | - | NC_000001.11:g.117622972T>C | ExAC,gnomAD |
rs1173277102 | p.Ile35Val | missense variant | - | NC_000001.11:g.117622971A>G | TOPMed |
rs779398843 | p.Gly37Arg | missense variant | - | NC_000001.11:g.117622977G>A | ExAC,TOPMed,gnomAD |
rs921184290 | p.Arg38Ter | stop gained | - | NC_000001.11:g.117622980C>T | TOPMed |
rs148397151 | p.Arg38Gln | missense variant | - | NC_000001.11:g.117622981G>A | ESP,ExAC,TOPMed,gnomAD |
rs921184290 | p.Arg38Ter | stop gained | - | NC_000001.11:g.117622980C>T | NCI-TCGA |
NCI-TCGA novel | p.Gly39Ala | missense variant | - | NC_000001.11:g.117622984G>C | NCI-TCGA |
rs772518025 | p.Asn40Lys | missense variant | - | NC_000001.11:g.117622988C>G | ExAC,gnomAD |
NCI-TCGA novel | p.Asn40Ser | missense variant | - | NC_000001.11:g.117622987A>G | NCI-TCGA |
rs1378831831 | p.Phe41Val | missense variant | - | NC_000001.11:g.117622989T>G | TOPMed |
COSM3471992 | p.Pro42Ser | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117622992C>T | NCI-TCGA Cosmic |
rs953053109 | p.Leu44Val | missense variant | - | NC_000001.11:g.117622998T>G | gnomAD |
rs773602227 | p.Glu45Gln | missense variant | - | NC_000001.11:g.117623001G>C | ExAC,gnomAD |
rs1230332453 | p.Ile46Thr | missense variant | - | NC_000001.11:g.117623005T>C | gnomAD |
rs747161845 | p.Ile46Val | missense variant | - | NC_000001.11:g.117623004A>G | ExAC,gnomAD |
rs1186011113 | p.Asp50Asn | missense variant | - | NC_000001.11:g.117623016G>A | TOPMed |
rs538766512 | p.Val52Ile | missense variant | - | NC_000001.11:g.117623022G>A | 1000Genomes,ExAC,gnomAD |
rs538766512 | p.Val52Ile | missense variant | - | NC_000001.11:g.117623022G>A | NCI-TCGA,NCI-TCGA Cosmic |
rs553880208 | p.Gln53Pro | missense variant | - | NC_000001.11:g.117623026A>C | 1000Genomes,ExAC,TOPMed,gnomAD |
rs775316333 | p.Thr54Ile | missense variant | - | NC_000001.11:g.117623029C>T | ExAC,gnomAD |
rs763834209 | p.Val55Ile | missense variant | - | NC_000001.11:g.117623031G>A | ExAC,gnomAD |
rs565811357 | p.Arg56Leu | missense variant | - | NC_000001.11:g.117623035G>T | 1000Genomes,ExAC,TOPMed,gnomAD |
rs565811357 | p.Arg56His | missense variant | - | NC_000001.11:g.117623035G>A | 1000Genomes,ExAC,TOPMed,gnomAD |
rs565811357 | p.Arg56His | missense variant | - | NC_000001.11:g.117623035G>A | NCI-TCGA,NCI-TCGA Cosmic |
rs756798728 | p.Arg56Cys | missense variant | - | NC_000001.11:g.117623034C>T | ExAC,gnomAD |
rs755549163 | p.Ser57Arg | missense variant | - | NC_000001.11:g.117623039T>A | ExAC,gnomAD |
rs768091631 | p.Arg58Trp | missense variant | - | NC_000001.11:g.117623040C>T | ExAC,TOPMed,gnomAD |
rs776281952 | p.Arg58Gln | missense variant | - | NC_000001.11:g.117623041G>A | TOPMed,gnomAD |
rs1630312 | p.His67Gln | missense variant | - | NC_000001.11:g.117623069C>G | UniProt,dbSNP |
VAR_060132 | p.His67Gln | missense variant | - | NC_000001.11:g.117623069C>G | UniProt |
rs1630312 | p.His67Gln | missense variant | - | NC_000001.11:g.117623069C>G | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
RCV000120902 | p.His67Gln | missense variant | - | NC_000001.11:g.117623069C>G | ClinVar |
rs758840994 | p.His67Arg | missense variant | - | NC_000001.11:g.117623068A>G | ExAC,gnomAD |
rs771057074 | p.Asp68Asn | missense variant | - | NC_000001.11:g.117623070G>A | ExAC,gnomAD |
rs745917069 | p.Val69Ile | missense variant | - | NC_000001.11:g.117623073G>A | NCI-TCGA,NCI-TCGA Cosmic |
rs745917069 | p.Val69Ile | missense variant | - | NC_000001.11:g.117623073G>A | ExAC,TOPMed,gnomAD |
rs1432369724 | p.Arg70Trp | missense variant | - | NC_000001.11:g.117623076C>T | NCI-TCGA Cosmic |
rs1432369724 | p.Arg70Trp | missense variant | - | NC_000001.11:g.117623076C>T | TOPMed |
rs762807647 | p.Asn72Asp | missense variant | - | NC_000001.11:g.117623082A>G | ExAC,gnomAD |
rs1355231501 | p.Asn72Ser | missense variant | - | NC_000001.11:g.117623083A>G | gnomAD |
rs1278971822 | p.Ala75Thr | missense variant | - | NC_000001.11:g.117623091G>A | gnomAD |
rs1278971822 | p.Ala75Thr | missense variant | - | NC_000001.11:g.117623091G>A | NCI-TCGA |
rs1211776583 | p.Val79Ile | missense variant | - | NC_000001.11:g.117623103G>A | gnomAD |
rs1165810632 | p.Lys82Arg | missense variant | - | NC_000001.11:g.117623113A>G | TOPMed |
rs767046262 | p.Leu86Phe | missense variant | - | NC_000001.11:g.117623126G>T | ExAC,gnomAD |
rs1385230345 | p.Gly87Val | missense variant | - | NC_000001.11:g.117623128G>T | TOPMed |
rs765921039 | p.Cys88Phe | missense variant | - | NC_000001.11:g.117623131G>T | ExAC,gnomAD |
rs139168147 | p.Leu93Val | missense variant | - | NC_000001.11:g.117623145C>G | ESP,ExAC,TOPMed,gnomAD |
rs1354348705 | p.Ile94Thr | missense variant | - | NC_000001.11:g.117623149T>C | gnomAD |
rs757552843 | p.Phe95Leu | missense variant | - | NC_000001.11:g.117623153C>G | ExAC,gnomAD |
rs1371399685 | p.Phe95Ser | missense variant | - | NC_000001.11:g.117623152T>C | gnomAD |
rs751943358 | p.Phe95Leu | missense variant | - | NC_000001.11:g.117623151T>C | ExAC,TOPMed,gnomAD |
rs781294756 | p.His96Leu | missense variant | - | NC_000001.11:g.117623155A>T | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.His96MetPheSerTerUnkUnk | frameshift | - | NC_000001.11:g.117623153C>- | NCI-TCGA |
rs190981033 | p.His96Gln | missense variant | - | NC_000001.11:g.117623156T>G | 1000Genomes,ExAC,gnomAD |
rs781294756 | p.His96Arg | missense variant | - | NC_000001.11:g.117623155A>G | ExAC,TOPMed,gnomAD |
rs1293686110 | p.Ala98Pro | missense variant | - | NC_000001.11:g.117623160G>C | TOPMed |
rs1302106502 | p.Leu99Phe | missense variant | - | NC_000001.11:g.117623163C>T | gnomAD |
NCI-TCGA novel | p.Pro100Ser | missense variant | - | NC_000001.11:g.117623166C>T | NCI-TCGA |
rs893973707 | p.Phe105Leu | missense variant | - | NC_000001.11:g.117623181T>C | gnomAD |
COSM116444 | p.Gln106Leu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623185A>T | NCI-TCGA Cosmic |
COSM3862349 | p.Gln106Ter | stop gained | Variant assessed as Somatic; HIGH impact. | NC_000001.11:g.117623184C>T | NCI-TCGA Cosmic |
rs1358461933 | p.Leu107Val | missense variant | - | NC_000001.11:g.117623187C>G | TOPMed |
rs769764155 | p.Val108Ile | missense variant | - | NC_000001.11:g.117623190G>A | ExAC,gnomAD |
rs951158173 | p.Asp110Asn | missense variant | - | NC_000001.11:g.117623196G>A | TOPMed |
NCI-TCGA novel | p.Asp110Tyr | missense variant | - | NC_000001.11:g.117623196G>T | NCI-TCGA |
rs1196590539 | p.Leu113Pro | missense variant | - | NC_000001.11:g.117623206T>C | gnomAD |
NCI-TCGA novel | p.Leu113Met | missense variant | - | NC_000001.11:g.117623205C>A | NCI-TCGA |
rs780049033 | p.Ser115Cys | missense variant | - | NC_000001.11:g.117623212C>G | ExAC,gnomAD |
rs780049033 | p.Ser115Phe | missense variant | - | NC_000001.11:g.117623212C>T | NCI-TCGA Cosmic |
rs780049033 | p.Ser115Phe | missense variant | - | NC_000001.11:g.117623212C>T | ExAC,gnomAD |
COSM4990424 | p.Leu116Phe | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623214C>T | NCI-TCGA Cosmic |
rs371789381 | p.Asn118Asp | missense variant | - | NC_000001.11:g.117623220A>G | ESP,ExAC,TOPMed,gnomAD |
rs556415905 | p.Asn118Lys | missense variant | - | NC_000001.11:g.117623222C>A | 1000Genomes,ExAC,TOPMed,gnomAD |
rs556415905 | p.Asn118Lys | missense variant | - | NC_000001.11:g.117623222C>G | 1000Genomes,ExAC,TOPMed,gnomAD |
rs774169628 | p.Phe119Leu | missense variant | - | NC_000001.11:g.117623223T>C | ExAC,gnomAD |
rs1303373643 | p.Phe119Ser | missense variant | - | NC_000001.11:g.117623224T>C | TOPMed |
COSM4021140 | p.Pro121Ser | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623229C>T | NCI-TCGA Cosmic |
COSM4414269 | p.Pro121Ala | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623229C>G | NCI-TCGA Cosmic |
rs1191996445 | p.Pro121Leu | missense variant | - | NC_000001.11:g.117623230C>T | gnomAD |
rs1419000325 | p.Glu122Val | missense variant | - | NC_000001.11:g.117623233A>T | gnomAD |
rs1419000325 | p.Glu122Gly | missense variant | - | NC_000001.11:g.117623233A>G | gnomAD |
rs1476955055 | p.Gly123Ser | missense variant | - | NC_000001.11:g.117623235G>A | TOPMed,gnomAD |
rs1349639622 | p.Gly123Val | missense variant | - | NC_000001.11:g.117623236G>T | TOPMed |
rs1476955055 | p.Gly123Cys | missense variant | - | NC_000001.11:g.117623235G>T | TOPMed,gnomAD |
rs1476955055 | p.Gly123Ser | missense variant | - | NC_000001.11:g.117623235G>A | NCI-TCGA |
NCI-TCGA novel | p.Asn125Ser | missense variant | - | NC_000001.11:g.117623242A>G | NCI-TCGA |
rs761490678 | p.Lys128Arg | missense variant | - | NC_000001.11:g.117623251A>G | ExAC,gnomAD |
NCI-TCGA novel | p.Ile129Asn | missense variant | - | NC_000001.11:g.117623254T>A | NCI-TCGA |
rs774747996 | p.Pro131Leu | missense variant | - | NC_000001.11:g.117623260C>T | ExAC,gnomAD |
rs1420340818 | p.Val132Ile | missense variant | - | NC_000001.11:g.117623262G>A | TOPMed |
rs1322105910 | p.Thr133Ser | missense variant | - | NC_000001.11:g.117623266C>G | gnomAD |
rs1461402036 | p.Thr133Ala | missense variant | - | NC_000001.11:g.117623265A>G | gnomAD |
rs965004236 | p.Ala137Val | missense variant | - | NC_000001.11:g.117623278C>T | TOPMed |
rs772744645 | p.Ala137Thr | missense variant | - | NC_000001.11:g.117623277G>A | ExAC,gnomAD |
rs766046722 | p.Val139Met | missense variant | - | NC_000001.11:g.117623283G>A | ExAC,gnomAD |
rs376181122 | p.Gln140Arg | missense variant | - | NC_000001.11:g.117623287A>G | ESP,ExAC,TOPMed,gnomAD |
rs781549053 | p.Thr147Met | missense variant | - | NC_000001.11:g.117623308C>T | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Asp148Gly | missense variant | - | NC_000001.11:g.117623311A>G | NCI-TCGA |
rs145001981 | p.Thr149Ile | missense variant | - | NC_000001.11:g.117623314C>T | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs749332682 | p.Arg151Leu | missense variant | - | NC_000001.11:g.117623320G>T | ExAC,TOPMed,gnomAD |
rs749332682 | p.Arg151His | missense variant | - | NC_000001.11:g.117623320G>A | ExAC,TOPMed,gnomAD |
rs780173405 | p.Arg151Ser | missense variant | - | NC_000001.11:g.117623319C>A | ExAC,TOPMed,gnomAD |
rs780173405 | p.Arg151Cys | missense variant | - | NC_000001.11:g.117623319C>T | NCI-TCGA |
rs780173405 | p.Arg151Cys | missense variant | - | NC_000001.11:g.117623319C>T | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Ser158Phe | missense variant | - | NC_000001.11:g.117623341C>T | NCI-TCGA |
rs201507664 | p.Asn159Tyr | missense variant | - | NC_000001.11:g.117623343A>T | 1000Genomes,ExAC,gnomAD |
rs1422217522 | p.Lys160Asn | missense variant | - | NC_000001.11:g.117623348G>T | TOPMed,gnomAD |
rs1359326657 | p.Gly162Arg | missense variant | - | NC_000001.11:g.117623352G>A | TOPMed,gnomAD |
NCI-TCGA novel | p.Asn164Ile | missense variant | - | NC_000001.11:g.117623359A>T | NCI-TCGA |
rs746707589 | p.Val165Met | missense variant | - | NC_000001.11:g.117623361G>A | ExAC,gnomAD |
rs1170591104 | p.Phe169Ser | missense variant | - | NC_000001.11:g.117623374T>C | TOPMed |
rs776332343 | p.Val170Ala | missense variant | - | NC_000001.11:g.117623377T>C | ExAC,gnomAD |
rs1282197258 | p.Val170Phe | missense variant | - | NC_000001.11:g.117623376G>T | gnomAD |
rs147179158 | p.Asp171Asn | missense variant | - | NC_000001.11:g.117623379G>A | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs147179158 | p.Asp171Asn | missense variant | - | NC_000001.11:g.117623379G>A | NCI-TCGA |
rs762319543 | p.Ile173Thr | missense variant | - | NC_000001.11:g.117623386T>C | ExAC,gnomAD |
rs767827215 | p.Arg174Trp | missense variant | - | NC_000001.11:g.117623388C>T | NCI-TCGA |
rs750792861 | p.Arg174Gln | missense variant | - | NC_000001.11:g.117623389G>A | NCI-TCGA,NCI-TCGA Cosmic |
rs750792861 | p.Arg174Gln | missense variant | - | NC_000001.11:g.117623389G>A | ExAC,TOPMed |
rs767827215 | p.Arg174Trp | missense variant | - | NC_000001.11:g.117623388C>T | ExAC,TOPMed,gnomAD |
rs756366617 | p.Arg175Cys | missense variant | - | NC_000001.11:g.117623391C>T | ExAC,gnomAD |
rs756366617 | p.Arg175Cys | missense variant | - | NC_000001.11:g.117623391C>T | NCI-TCGA |
rs1185953882 | p.Gln176His | missense variant | - | NC_000001.11:g.117623396G>T | gnomAD |
rs1431680747 | p.Ser180Gly | missense variant | - | NC_000001.11:g.117623406A>G | gnomAD |
rs1239549020 | p.Val181Ala | missense variant | - | NC_000001.11:g.117623410T>C | gnomAD |
rs1379186922 | p.Phe184Val | missense variant | - | NC_000001.11:g.117623418T>G | gnomAD |
rs1277828975 | p.Ile186Val | missense variant | - | NC_000001.11:g.117623424A>G | gnomAD |
rs754010269 | p.Ile187Asn | missense variant | - | NC_000001.11:g.117623428T>A | ExAC,gnomAD |
rs766564274 | p.Ile187Phe | missense variant | - | NC_000001.11:g.117623427A>T | ExAC,gnomAD |
NCI-TCGA novel | p.Ser190Phe | missense variant | - | NC_000001.11:g.117623437C>T | NCI-TCGA |
rs748094673 | p.Leu191Phe | missense variant | - | NC_000001.11:g.117623441G>C | ExAC,gnomAD |
NCI-TCGA novel | p.Phe194Leu | missense variant | - | NC_000001.11:g.117623450C>G | NCI-TCGA |
rs373419973 | p.Tyr195Cys | missense variant | - | NC_000001.11:g.117623452A>G | ESP,ExAC,TOPMed,gnomAD |
rs746800316 | p.Cys197Arg | missense variant | - | NC_000001.11:g.117623457T>C | ExAC,gnomAD |
rs770804707 | p.Asn199Ser | missense variant | - | NC_000001.11:g.117623464A>G | ExAC,gnomAD |
rs776457933 | p.Asn200Ser | missense variant | - | NC_000001.11:g.117623467A>G | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Pro201Ser | missense variant | - | NC_000001.11:g.117623469C>T | NCI-TCGA |
NCI-TCGA novel | p.Pro201Leu | missense variant | - | NC_000001.11:g.117623470C>T | NCI-TCGA |
rs745444038 | p.Pro201Thr | missense variant | - | NC_000001.11:g.117623469C>A | ExAC,TOPMed,gnomAD |
rs1310015046 | p.Pro208Arg | missense variant | - | NC_000001.11:g.117623491C>G | TOPMed |
rs775048736 | p.Thr209Ser | missense variant | - | NC_000001.11:g.117623493A>T | ExAC,gnomAD |
rs773496649 | p.Ile211Thr | missense variant | - | NC_000001.11:g.117623500T>C | ExAC,gnomAD |
rs1181723324 | p.Ile211Phe | missense variant | - | NC_000001.11:g.117623499A>T | gnomAD |
NCI-TCGA novel | p.Gly212Arg | missense variant | - | NC_000001.11:g.117623502G>A | NCI-TCGA |
rs1442073130 | p.Met215Thr | missense variant | - | NC_000001.11:g.117623512T>C | gnomAD |
rs766689047 | p.Gly217Arg | missense variant | - | NC_000001.11:g.117623517G>A | ExAC,gnomAD |
COSM3471996 | p.Asp218Asn | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623520G>A | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Glu221ValPheSerTerUnkUnk | frameshift | - | NC_000001.11:g.117623529_117623530insTTGGGGACCACTGGTGTGGC | NCI-TCGA |
rs754073638 | p.Ala222Asp | missense variant | - | NC_000001.11:g.117623533C>A | ExAC,gnomAD |
NCI-TCGA novel | p.Asp224Asn | missense variant | - | NC_000001.11:g.117623538G>A | NCI-TCGA |
rs377384965 | p.Asp224Glu | missense variant | - | NC_000001.11:g.117623540C>A | ESP,ExAC,TOPMed,gnomAD |
rs1331321666 | p.Gln227Arg | missense variant | - | NC_000001.11:g.117623548A>G | TOPMed |
rs371434677 | p.Ala232Thr | missense variant | - | NC_000001.11:g.117623562G>A | NCI-TCGA |
rs752792421 | p.Ala232Val | missense variant | - | NC_000001.11:g.117623563C>T | ExAC,TOPMed,gnomAD |
rs371434677 | p.Ala232Ser | missense variant | - | NC_000001.11:g.117623562G>T | ESP,gnomAD |
rs371434677 | p.Ala232Thr | missense variant | - | NC_000001.11:g.117623562G>A | ESP,gnomAD |
rs1337416217 | p.Lys234Asn | missense variant | - | NC_000001.11:g.117623570G>C | TOPMed |
rs1310140275 | p.Asn235Ser | missense variant | - | NC_000001.11:g.117623572A>G | gnomAD |
rs1231378622 | p.Pro236Thr | missense variant | - | NC_000001.11:g.117623574C>A | gnomAD |
rs1198478524 | p.Gly242Glu | missense variant | - | NC_000001.11:g.117623593G>A | gnomAD |
NCI-TCGA novel | p.Gly242Arg | missense variant | - | NC_000001.11:g.117623592G>A | NCI-TCGA |
rs757126681 | p.Leu244Phe | missense variant | - | NC_000001.11:g.117623598C>T | ExAC,gnomAD |
COSM2156513 | p.Leu244Val | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623598C>G | NCI-TCGA Cosmic |
rs745570371 | p.Asn249Ser | missense variant | - | NC_000001.11:g.117623614A>G | ExAC,gnomAD |
rs769480797 | p.Leu251Phe | missense variant | - | NC_000001.11:g.117623619C>T | ExAC,gnomAD |
rs915278770 | p.Val252Leu | missense variant | - | NC_000001.11:g.117623622G>C | TOPMed |
rs779467652 | p.Arg253Gln | missense variant | - | NC_000001.11:g.117623626G>A | NCI-TCGA,NCI-TCGA Cosmic |
rs779467652 | p.Arg253Gln | missense variant | - | NC_000001.11:g.117623626G>A | ExAC,TOPMed,gnomAD |
rs1379420313 | p.Arg253Trp | missense variant | - | NC_000001.11:g.117623625C>T | TOPMed |
rs1462556539 | p.Asp254Asn | missense variant | - | NC_000001.11:g.117623628G>A | TOPMed |
rs587778306 | p.Thr258Ile | missense variant | - | NC_000001.11:g.117623641C>T | gnomAD |
RCV000120903 | p.Thr258Ile | missense variant | - | NC_000001.11:g.117623641C>T | ClinVar |
RCV000120906 | p.Asp259Tyr | missense variant | - | NC_000001.11:g.117623643G>T | ClinVar |
rs587778308 | p.Asp259Tyr | missense variant | - | NC_000001.11:g.117623643G>T | - |
COSM3788499 | p.Asp259His | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623643G>C | NCI-TCGA Cosmic |
COSM1688388 | p.Glu261Lys | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623649G>A | NCI-TCGA Cosmic |
COSM894532 | p.Glu262Asp | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623654A>C | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Glu262Ter | stop gained | - | NC_000001.11:g.117623652G>T | NCI-TCGA |
NCI-TCGA novel | p.Ile263Leu | missense variant | - | NC_000001.11:g.117623655A>C | NCI-TCGA |
NCI-TCGA novel | p.Ile263Met | missense variant | - | NC_000001.11:g.117623657C>G | NCI-TCGA |
NCI-TCGA novel | p.Lys264Arg | missense variant | - | NC_000001.11:g.117623659A>G | NCI-TCGA |
rs1487005772 | p.Glu267Gln | missense variant | - | NC_000001.11:g.117623667G>C | gnomAD |
rs761103312 | p.Arg268Cys | missense variant | - | NC_000001.11:g.117623670C>T | ExAC,TOPMed,gnomAD |
rs754072349 | p.Arg268His | missense variant | - | NC_000001.11:g.117623671G>A | ExAC,TOPMed,gnomAD |
rs1239289962 | p.Met270Val | missense variant | - | NC_000001.11:g.117623676A>G | TOPMed |
COSM894533 | p.Phe274Leu | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623688T>C | NCI-TCGA Cosmic |
NCI-TCGA novel | p.Phe275Tyr | missense variant | - | NC_000001.11:g.117623692T>A | NCI-TCGA |
NCI-TCGA novel | p.Ile276ProPheSerTerUnkUnk | frameshift | - | NC_000001.11:g.117623693_117623694insCCGTTCTTGTTGG | NCI-TCGA |
rs778618300 | p.Pro279Leu | missense variant | - | NC_000001.11:g.117623704C>T | ExAC,TOPMed,gnomAD |
RCV000120901 | p.Ile281Val | missense variant | - | NC_000001.11:g.117623709A>G | ClinVar |
rs77871185 | p.Ile281Val | missense variant | - | NC_000001.11:g.117623709A>G | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs764017740 | p.Leu282Val | missense variant | - | NC_000001.11:g.117623712C>G | ExAC,gnomAD |
rs1219813462 | p.Arg286Lys | missense variant | - | NC_000001.11:g.117623725G>A | gnomAD |
rs758092069 | p.Leu288Val | missense variant | - | NC_000001.11:g.117623730T>G | TOPMed,gnomAD |
rs764728855 | p.Tyr291Ter | stop gained | - | NC_000001.11:g.117623740dup | ExAC,gnomAD |
rs149654076 | p.Ala297Thr | missense variant | - | NC_000001.11:g.117623757G>A | NCI-TCGA,NCI-TCGA Cosmic |
rs149654076 | p.Ala297Pro | missense variant | - | NC_000001.11:g.117623757G>C | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs149654076 | p.Ala297Thr | missense variant | - | NC_000001.11:g.117623757G>A | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
RCV000120907 | p.Ala297Thr | missense variant | - | NC_000001.11:g.117623757G>A | ClinVar |
rs145471785 | p.Glu299Lys | missense variant | - | NC_000001.11:g.117623763G>A | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
RCV000120908 | p.Glu299Lys | missense variant | - | NC_000001.11:g.117623763G>A | ClinVar |
rs768215715 | p.Ser302Asn | missense variant | - | NC_000001.11:g.117623773G>A | ExAC,TOPMed,gnomAD |
rs538158859 | p.Ser302Gly | missense variant | - | NC_000001.11:g.117623772A>G | 1000Genomes,ExAC,gnomAD |
rs538158859 | p.Ser302Arg | missense variant | - | NC_000001.11:g.117623772A>C | 1000Genomes,ExAC,gnomAD |
rs747582052 | p.Lys303Gln | missense variant | - | NC_000001.11:g.117623775A>C | ExAC,gnomAD |
rs1391512260 | p.Asp305Asn | missense variant | - | NC_000001.11:g.117623781G>A | TOPMed,gnomAD |
rs1312455607 | p.Met308Ile | missense variant | - | NC_000001.11:g.117623792G>C | gnomAD |
rs770016455 | p.Met308Thr | missense variant | - | NC_000001.11:g.117623791T>C | ExAC,gnomAD |
rs150740852 | p.Met308Leu | missense variant | - | NC_000001.11:g.117623790A>C | ESP,ExAC,TOPMed,gnomAD |
rs150740852 | p.Met308Val | missense variant | - | NC_000001.11:g.117623790A>G | ESP,ExAC,TOPMed,gnomAD |
rs372516345 | p.Ile309Thr | missense variant | - | NC_000001.11:g.117623794T>C | ESP,TOPMed |
rs775789017 | p.Arg311Cys | missense variant | - | NC_000001.11:g.117623799C>T | NCI-TCGA,NCI-TCGA Cosmic |
rs775789017 | p.Arg311Cys | missense variant | - | NC_000001.11:g.117623799C>T | ExAC,TOPMed,gnomAD |
COSM3471998 | p.Arg312Met | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623803G>T | NCI-TCGA Cosmic |
rs764287568 | p.Glu316Lys | missense variant | - | NC_000001.11:g.117623814G>A | ExAC,TOPMed,gnomAD |
rs764287568 | p.Glu316Lys | missense variant | - | NC_000001.11:g.117623814G>A | NCI-TCGA |
rs1215452754 | p.Thr318Ala | missense variant | - | NC_000001.11:g.117623820A>G | gnomAD |
NCI-TCGA novel | p.Val319Leu | missense variant | - | NC_000001.11:g.117623823G>T | NCI-TCGA |
rs767537718 | p.Val319Met | missense variant | - | NC_000001.11:g.117623823G>A | ExAC,TOPMed,gnomAD |
rs1186956228 | p.Gly323Glu | missense variant | - | NC_000001.11:g.117623836G>A | gnomAD |
rs1186956228 | p.Gly323Glu | missense variant | - | NC_000001.11:g.117623836G>A | NCI-TCGA Cosmic |
rs755966473 | p.Arg326Leu | missense variant | - | NC_000001.11:g.117623845G>T | ExAC,gnomAD |
rs755966473 | p.Arg326His | missense variant | - | NC_000001.11:g.117623845G>A | ExAC,gnomAD |
rs750335875 | p.Arg326Cys | missense variant | - | NC_000001.11:g.117623844C>T | ExAC,gnomAD |
rs1281807855 | p.Ile333Phe | missense variant | - | NC_000001.11:g.117623865A>T | TOPMed,gnomAD |
COSM3472000 | p.Ser334Phe | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623869C>T | NCI-TCGA Cosmic |
rs1383000604 | p.Ser334Cys | missense variant | - | NC_000001.11:g.117623869C>G | TOPMed |
rs753542382 | p.Arg339His | missense variant | - | NC_000001.11:g.117623884G>A | ExAC,TOPMed,gnomAD |
rs376774297 | p.Ala342Val | missense variant | - | NC_000001.11:g.117623893C>T | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Asn345LysPheSerTerUnkUnk | frameshift | - | NC_000001.11:g.117623903C>- | NCI-TCGA |
rs930666933 | p.Ile346Val | missense variant | - | NC_000001.11:g.117623904A>G | TOPMed,gnomAD |
rs1238866114 | p.Ile347Leu | missense variant | - | NC_000001.11:g.117623907A>C | gnomAD |
rs747636778 | p.Ser349Cys | missense variant | - | NC_000001.11:g.117623913A>T | ExAC,gnomAD |
rs1355458797 | p.Ser349Asn | missense variant | - | NC_000001.11:g.117623914G>A | gnomAD |
rs757856198 | p.Asn352Ser | missense variant | - | NC_000001.11:g.117623923A>G | ExAC,TOPMed,gnomAD |
rs74114325 | p.Val353Ile | missense variant | - | NC_000001.11:g.117623925G>A | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs557599465 | p.Pro359Leu | missense variant | - | NC_000001.11:g.117623944C>T | TOPMed,gnomAD |
rs557599465 | p.Pro359Leu | missense variant | - | NC_000001.11:g.117623944C>T | NCI-TCGA |
rs1354785362 | p.Pro361Leu | missense variant | - | NC_000001.11:g.117623950C>T | TOPMed |
COSM3862351 | p.Pro361Ser | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.117623949C>T | NCI-TCGA Cosmic |
rs773285739 | p.Val363Ile | missense variant | - | NC_000001.11:g.117623955G>A | ExAC,TOPMed,gnomAD |
rs773285739 | p.Val363Ile | missense variant | - | NC_000001.11:g.117623955G>A | NCI-TCGA,NCI-TCGA Cosmic |
rs773285739 | p.Val363Phe | missense variant | - | NC_000001.11:g.117623955G>T | ExAC,TOPMed,gnomAD |
rs760471278 | p.Asp365Ala | missense variant | - | NC_000001.11:g.117623962A>C | ExAC |
NCI-TCGA novel | p.Asp365Asn | missense variant | - | NC_000001.11:g.117623961G>A | NCI-TCGA |
rs1256168715 | p.Asn367Thr | missense variant | - | NC_000001.11:g.117623968A>C | TOPMed,gnomAD |
rs1400295239 | p.Ser369Asn | missense variant | - | NC_000001.11:g.117623974G>A | gnomAD |
rs753546205 | p.Asn370Lys | missense variant | - | NC_000001.11:g.117623978C>G | ExAC,gnomAD |
rs754709388 | p.Tyr372His | missense variant | - | NC_000001.11:g.117623982T>C | ExAC,gnomAD |
rs752308622 | p.Val373Ile | missense variant | - | NC_000001.11:g.117623985G>A | ExAC,gnomAD |
rs1345951307 | p.Ala374Val | missense variant | - | NC_000001.11:g.117623989C>T | TOPMed |
NCI-TCGA novel | p.Pro377Ser | missense variant | - | NC_000001.11:g.117623997C>T | NCI-TCGA |
rs1212041385 | p.Val378Ile | missense variant | - | NC_000001.11:g.117624000G>A | gnomAD |
rs746449090 | p.Tyr380Asp | missense variant | - | NC_000001.11:g.117624006T>G | ExAC,TOPMed,gnomAD |
rs746449090 | p.Tyr380His | missense variant | - | NC_000001.11:g.117624006T>C | ExAC,TOPMed,gnomAD |
rs1185278454 | p.Ser381Arg | missense variant | - | NC_000001.11:g.117624009A>C | gnomAD |
rs780504872 | p.Gln382His | missense variant | - | NC_000001.11:g.117624014G>C | ExAC,gnomAD |
rs749590706 | p.Tyr384Cys | missense variant | - | NC_000001.11:g.117624019A>G | ExAC,TOPMed,gnomAD |
rs769091230 | p.Pro385His | missense variant | - | NC_000001.11:g.117624022C>A | ExAC |
rs774743199 | p.Trp387Cys | missense variant | - | NC_000001.11:g.117624029G>C | ExAC,TOPMed,gnomAD |
rs774743199 | p.Trp387Ter | stop gained | - | NC_000001.11:g.117624029G>A | ExAC,TOPMed,gnomAD |
rs774743199 | p.Trp387Cys | missense variant | - | NC_000001.11:g.117624029G>T | ExAC,TOPMed,gnomAD |
rs774743199 | p.Trp387Ter | stop gained | - | NC_000001.11:g.117624029G>A | NCI-TCGA |
rs1423398747 | p.Pro389Arg | missense variant | - | NC_000001.11:g.117624034C>G | TOPMed,gnomAD |
rs1423398747 | p.Pro389Leu | missense variant | - | NC_000001.11:g.117624034C>T | TOPMed,gnomAD |