rs1466076982 | p.Asn2Tyr | missense variant | - | NC_000001.11:g.9872061T>A | gnomAD |
rs771836718 | p.Asn2Lys | missense variant | - | NC_000001.11:g.9872059G>T | ExAC,gnomAD |
rs150360638 | p.Arg3Leu | missense variant | - | NC_000001.11:g.9872057C>A | ESP,ExAC,TOPMed,gnomAD |
rs150360638 | p.Arg3His | missense variant | - | NC_000001.11:g.9872057C>T | ESP,ExAC,TOPMed,gnomAD |
rs147067665 | p.Arg3Cys | missense variant | - | NC_000001.11:g.9872058G>A | ESP,ExAC,TOPMed,gnomAD |
rs1183573009 | p.Glu4Asp | missense variant | - | NC_000001.11:g.9872053C>G | TOPMed |
rs1230381774 | p.Glu4Lys | missense variant | - | NC_000001.11:g.9872055C>T | TOPMed,gnomAD |
rs1330002148 | p.Gly5Val | missense variant | - | NC_000001.11:g.9872051C>A | gnomAD |
rs1299911882 | p.Ala6Val | missense variant | - | NC_000001.11:g.9872048G>A | TOPMed,gnomAD |
rs761797446 | p.Ala6Pro | missense variant | - | NC_000001.11:g.9872049C>G | ExAC,TOPMed,gnomAD |
rs113935062 | p.Gly8Arg | missense variant | - | NC_000001.11:g.9872043C>T | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs781302251 | p.Gly8Glu | missense variant | - | NC_000001.11:g.9872042C>T | ExAC,gnomAD |
rs113935062 | p.Gly8Arg | missense variant | - | NC_000001.11:g.9872043C>T | NCI-TCGA,NCI-TCGA Cosmic |
rs751743905 | p.Lys9Asn | missense variant | - | NC_000001.11:g.9872038C>A | ExAC,TOPMed,gnomAD |
rs777994158 | p.Pro11Leu | missense variant | - | NC_000001.11:g.9872033G>A | ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Glu12Gly | missense variant | - | NC_000001.11:g.9872030T>C | NCI-TCGA |
rs1189131001 | p.Glu13Asp | missense variant | - | NC_000001.11:g.9872026C>G | gnomAD |
rs753671543 | p.Met14Thr | missense variant | - | NC_000001.11:g.9872024A>G | ExAC,gnomAD |
rs1187640116 | p.Ile16Val | missense variant | - | NC_000001.11:g.9872019T>C | gnomAD |
rs1442815862 | p.Gln17Glu | missense variant | - | NC_000001.11:g.9872016G>C | TOPMed,gnomAD |
rs1442815862 | p.Gln17Ter | stop gained | - | NC_000001.11:g.9872016G>A | NCI-TCGA Cosmic |
rs1442815862 | p.Gln17Ter | stop gained | - | NC_000001.11:g.9872016G>A | TOPMed,gnomAD |
rs1257745822 | p.Gln17His | missense variant | - | NC_000001.11:g.9872014C>A | gnomAD |
rs1343663953 | p.Gln18Pro | missense variant | - | NC_000001.11:g.9872012T>G | gnomAD |
rs367851454 | p.Gln18Ter | stop gained | - | NC_000001.11:g.9872013G>A | ESP,ExAC,gnomAD |
rs760722655 | p.Lys19Arg | missense variant | - | NC_000001.11:g.9872009T>C | ExAC,gnomAD |
rs761438511 | p.Arg21Gln | missense variant | - | NC_000001.11:g.9872003C>T | ExAC,TOPMed,gnomAD |
rs761438511 | p.Arg21Leu | missense variant | - | NC_000001.11:g.9872003C>A | ExAC,TOPMed,gnomAD |
rs749931176 | p.Arg21Ter | stop gained | - | NC_000001.11:g.9872004G>A | ExAC,TOPMed,gnomAD |
rs774094632 | p.Val22Met | missense variant | - | NC_000001.11:g.9872001C>T | ExAC,gnomAD |
rs763818220 | p.Val22Ala | missense variant | - | NC_000001.11:g.9872000A>G | ExAC,gnomAD |
NCI-TCGA novel | p.Leu24Ile | missense variant | - | NC_000001.11:g.9871995G>T | NCI-TCGA |
rs1397261310 | p.Met25Val | missense variant | - | NC_000001.11:g.9871992T>C | TOPMed,gnomAD |
rs746418599 | p.Arg27Gln | missense variant | - | NC_000001.11:g.9871985C>T | ExAC,TOPMed,gnomAD |
rs770182367 | p.Arg27Trp | missense variant | - | NC_000001.11:g.9871986G>A | ExAC,TOPMed,gnomAD |
rs746418599 | p.Arg27Pro | missense variant | - | NC_000001.11:g.9871985C>G | ExAC,TOPMed,gnomAD |
COSM3493710 | p.Met29Thr | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.9871979A>G | NCI-TCGA Cosmic |
rs1388200557 | p.Gly30Arg | missense variant | - | NC_000001.11:g.9871977C>T | gnomAD |
rs777156046 | p.Gly30Glu | missense variant | - | NC_000001.11:g.9871976C>T | ExAC,gnomAD |
rs1209572072 | p.Leu33Val | missense variant | - | NC_000001.11:g.9871277G>C | gnomAD |
rs1330245872 | p.Leu33Arg | missense variant | - | NC_000001.11:g.9871276A>C | gnomAD |
rs1212238107 | p.Thr34Ala | missense variant | - | NC_000001.11:g.9871274T>C | TOPMed |
rs1275561036 | p.Glu37Val | missense variant | - | NC_000001.11:g.9871264T>A | gnomAD |
rs777066136 | p.Glu38Lys | missense variant | - | NC_000001.11:g.9871262C>T | ExAC,gnomAD |
NCI-TCGA novel | p.Glu38Gln | missense variant | - | NC_000001.11:g.9871262C>G | NCI-TCGA |
rs574333600 | p.Glu39Lys | missense variant | - | NC_000001.11:g.9871259C>T | 1000Genomes,ExAC,gnomAD |
rs201081336 | p.Arg42His | missense variant | - | NC_000001.11:g.9871249C>T | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
NCI-TCGA novel | p.Arg42Pro | missense variant | - | NC_000001.11:g.9871249C>G | NCI-TCGA |
rs773400948 | p.Arg42Cys | missense variant | - | NC_000001.11:g.9871250G>A | ExAC,gnomAD |
rs1410552050 | p.Tyr44Asp | missense variant | - | NC_000001.11:g.9871244A>C | gnomAD |
rs1191218589 | p.Tyr44Cys | missense variant | - | NC_000001.11:g.9871243T>C | gnomAD |
rs755922514 | p.Val47Leu | missense variant | - | NC_000001.11:g.9871235C>A | ExAC,TOPMed,gnomAD |
rs1241714108 | p.Asn49Ser | missense variant | - | NC_000001.11:g.9871228T>C | TOPMed |
rs745668650 | p.Asn49Asp | missense variant | - | NC_000001.11:g.9871229T>C | ExAC,gnomAD |
rs968654645 | p.Ser50Arg | missense variant | - | NC_000001.11:g.9871224G>C | TOPMed,gnomAD |
rs1022467751 | p.Ser53Asn | missense variant | - | NC_000001.11:g.9871216C>T | TOPMed |
rs1279634076 | p.Gln54Ter | stop gained | - | NC_000001.11:g.9871214G>A | gnomAD |
rs1201997978 | p.Leu55Pro | missense variant | - | NC_000001.11:g.9871210A>G | TOPMed |
rs757326660 | p.Pro57Leu | missense variant | - | NC_000001.11:g.9871204G>A | ExAC,TOPMed,gnomAD |
rs1273072507 | p.Ile60Thr | missense variant | - | NC_000001.11:g.9871195A>G | TOPMed |
rs1034308843 | p.Asp61Asn | missense variant | - | NC_000001.11:g.9871193C>T | TOPMed,gnomAD |
rs138271667 | p.Gln62His | missense variant | - | NC_000001.11:g.9871188C>A | 1000Genomes,ESP,ExAC,TOPMed,gnomAD |
rs1380242462 | p.Gly63Val | missense variant | - | NC_000001.11:g.9850776C>A | TOPMed |
rs1422513149 | p.Gly63Ser | missense variant | - | NC_000001.11:g.9871187C>T | gnomAD |
NCI-TCGA novel | p.Ala64Val | missense variant | - | NC_000001.11:g.9850773G>A | NCI-TCGA |
rs1179763132 | p.Asp66Asn | missense variant | - | NC_000001.11:g.9850768C>T | TOPMed |
rs548974391 | p.Val67Met | missense variant | - | NC_000001.11:g.9850765C>T | 1000Genomes,ExAC,gnomAD |
rs548974391 | p.Val67Leu | missense variant | - | NC_000001.11:g.9850765C>A | 1000Genomes,ExAC,gnomAD |
rs1371142601 | p.Val68Met | missense variant | - | NC_000001.11:g.9850762C>T | TOPMed,gnomAD |
COSM4010830 | p.Val68Ala | missense variant | Variant assessed as Somatic; MODERATE impact. | NC_000001.11:g.9850761A>G | NCI-TCGA Cosmic |
rs372414829 | p.Met69Leu | missense variant | - | NC_000001.11:g.9850759T>A | ESP,ExAC,TOPMed,gnomAD |
rs781187269 | p.Ser74Leu | missense variant | - | NC_000001.11:g.9850743G>A | ExAC,gnomAD |
rs199900946 | p.Thr76Arg | missense variant | - | NC_000001.11:g.9850737G>C | 1000Genomes,ExAC,TOPMed,gnomAD |
rs199900946 | p.Thr76Met | missense variant | - | NC_000001.11:g.9850737G>A | 1000Genomes,ExAC,TOPMed,gnomAD |
rs369249056 | p.Asp78Ala | missense variant | - | NC_000001.11:g.9850731T>G | ESP,ExAC,TOPMed,gnomAD |
rs778534202 | p.Arg79Gln | missense variant | - | NC_000001.11:g.9850728C>T | ExAC,gnomAD |
rs752154298 | p.Arg79Trp | missense variant | - | NC_000001.11:g.9850729G>A | ExAC,TOPMed,gnomAD |
rs1422466855 | p.Arg80Thr | missense variant | - | NC_000001.11:g.9850725C>G | gnomAD |
NCI-TCGA novel | p.Gln81Glu | missense variant | - | NC_000001.11:g.9850723G>C | NCI-TCGA |