Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.149482835G>ACA519057415IDSc.1564C>T (p.Leu522=)
c.931C>T (p.Leu311=)
c.1294C>T (p.Leu432=)
ClinVar dbSNP gnomAD v4
Xg.149482835G>CCA414517807IDSc.1564C>G (p.Leu522Val)
c.931C>G (p.Leu311Val)
c.1294C>G (p.Leu432Val)
gnomAD v4
Xg.149482835G>TCA414517808IDSc.1564C>A (p.Leu522Met)
c.931C>A (p.Leu311Met)
c.1294C>A (p.Leu432Met)
Xg.149482836T>ACA414517809IDSc.1563A>T (p.Glu521Asp)
c.930A>T (p.Glu310Asp)
c.1293A>T (p.Glu431Asp)
ClinVar dbSNP
Xg.149482836T>CCA519057416IDSc.1563A>G (p.Glu521=)
c.930A>G (p.Glu310=)
c.1293A>G (p.Glu431=)
Xg.149482836T>GCA414517810IDSc.1563A>C (p.Glu521Asp)
c.930A>C (p.Glu310Asp)
c.1293A>C (p.Glu431Asp)
Xg.149482836T=CA2465003948IDSc.1563A= (p.Glu521=)
c.930A= (p.Glu310=)
c.1293A= (p.Glu431=)
Xg.149482837delCA2695236480IDSc.1563del (p.Glu521AspfsTer28)
c.930del (p.Glu310AspfsTer28)
c.1293del (p.Glu431AspfsTer28)
Xg.149482837T>ACA414517813IDSc.1562A>T (p.Glu521Val)
c.929A>T (p.Glu310Val)
c.1292A>T (p.Glu431Val)
Xg.149482837T>CCA414517812IDSc.1562A>G (p.Glu521Gly)
c.929A>G (p.Glu310Gly)
c.1292A>G (p.Glu431Gly)
Xg.149482837T>GCA414517811IDSc.1562A>C (p.Glu521Ala)
c.929A>C (p.Glu310Ala)
c.1292A>C (p.Glu431Ala)
Xg.149482838C>ACA414517814IDSc.1561G>T (p.Glu521Ter)
c.928G>T (p.Glu310Ter)
c.1291G>T (p.Glu431Ter)
Xg.149482838C>GCA414517815IDSc.1561G>C (p.Glu521Gln)
c.928G>C (p.Glu310Gln)
c.1291G>C (p.Glu431Gln)
Xg.149482838C>TCA414517816IDSc.1561G>A (p.Glu521Lys)
c.928G>A (p.Glu310Lys)
c.1291G>A (p.Glu431Lys)
ClinVar dbSNP COSMIC
Xg.149482841dupCA2573159287IDSc.1561dup (p.Glu521GlyfsTer8)
c.928dup (p.Glu310GlyfsTer8)
c.1291dup (p.Glu431GlyfsTer8)
ClinVar dbSNP
Xg.149482841delCA2739289610IDSc.1561del (p.Glu521AsnfsTer28)
c.928del (p.Glu310AsnfsTer28)
c.1291del (p.Glu431AsnfsTer28)
Xg.149482839C>ACA519057417IDSc.1560G>T (p.Gly520=)
c.927G>T (p.Gly309=)
c.1290G>T (p.Gly430=)
Xg.149482839C=CA2465003949IDSc.1560G= (p.Gly520=)
c.927G= (p.Gly309=)
c.1290G= (p.Gly430=)
Xg.149482839C>GCA519057418IDSc.1560G>C (p.Gly520=)
c.927G>C (p.Gly309=)
c.1290G>C (p.Gly430=)
Xg.149482839C>TCA10537432IDSc.1560G>A (p.Gly520=)
c.927G>A (p.Gly309=)
c.1290G>A (p.Gly430=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.149482840C>ACA414517817IDSc.1559G>T (p.Gly520Val)
c.926G>T (p.Gly309Val)
c.1289G>T (p.Gly430Val)
Xg.149482840C>GCA414517818IDSc.1559G>C (p.Gly520Ala)
c.926G>C (p.Gly309Ala)
c.1289G>C (p.Gly430Ala)
Xg.149482840C>TCA414517819IDSc.1559G>A (p.Gly520Glu)
c.926G>A (p.Gly309Glu)
c.1289G>A (p.Gly430Glu)
Xg.149482841C>ACA414517820IDSc.1558G>T (p.Gly520Trp)
c.925G>T (p.Gly309Trp)
c.1288G>T (p.Gly430Trp)
Xg.149482841C>GCA414517821IDSc.1558G>C (p.Gly520Arg)
c.925G>C (p.Gly309Arg)
c.1288G>C (p.Gly430Arg)
Xg.149482841C>TCA414517822IDSc.1558G>A (p.Gly520Arg)
c.925G>A (p.Gly309Arg)
c.1288G>A (p.Gly430Arg)
Xg.149482842T>ACA519057419IDSc.1557A>T (p.Ala519=)
c.924A>T (p.Ala308=)
c.1287A>T (p.Ala429=)
Xg.149482842T>CCA519057420IDSc.1557A>G (p.Ala519=)
c.924A>G (p.Ala308=)
c.1287A>G (p.Ala429=)
Xg.149482842T>GCA519057421IDSc.1557A>C (p.Ala519=)
c.924A>C (p.Ala308=)
c.1287A>C (p.Ala429=)
Xg.149482843G>ACA414517823IDSc.1556C>T (p.Ala519Val)
c.923C>T (p.Ala308Val)
c.1286C>T (p.Ala429Val)
Xg.149482843G>CCA414517824IDSc.1556C>G (p.Ala519Gly)
c.923C>G (p.Ala308Gly)
c.1286C>G (p.Ala429Gly)
Xg.149482843G>TCA414517825IDSc.1556C>A (p.Ala519Glu)
c.923C>A (p.Ala308Glu)
c.1286C>A (p.Ala429Glu)
Xg.149482844C>ACA414517828IDSc.1555G>T (p.Ala519Ser)
c.922G>T (p.Ala308Ser)
c.1285G>T (p.Ala429Ser)
dbSNP gnomAD v3 gnomAD v4
Xg.149482844C=CA2465003950IDSc.1555G= (p.Ala519=)
c.922G= (p.Ala308=)
c.1285G= (p.Ala429=)
Xg.149482844C>GCA414517826IDSc.1555G>C (p.Ala519Pro)
c.922G>C (p.Ala308Pro)
c.1285G>C (p.Ala429Pro)
Xg.149482844C>TCA414517827IDSc.1555G>A (p.Ala519Thr)
c.922G>A (p.Ala308Thr)
c.1285G>A (p.Ala429Thr)
Xg.149482845A>CCA414517829IDSc.1554T>G (p.His518Gln)
c.921T>G (p.His307Gln)
c.1284T>G (p.His428Gln)
Xg.149482845A>GCA519057423IDSc.1554T>C (p.His518=)
c.921T>C (p.His307=)
c.1284T>C (p.His428=)
Xg.149482845A>TCA414517830IDSc.1554T>A (p.His518Gln)
c.921T>A (p.His307Gln)
c.1284T>A (p.His428Gln)
Xg.149482846T>ACA414517832IDSc.1553A>T (p.His518Leu)
c.920A>T (p.His307Leu)
c.1283A>T (p.His428Leu)
Xg.149482846T>CCA414517834IDSc.1553A>G (p.His518Arg)
c.920A>G (p.His307Arg)
c.1283A>G (p.His428Arg)
Xg.149482846T>GCA414517835IDSc.1553A>C (p.His518Pro)
c.920A>C (p.His307Pro)
c.1283A>C (p.His428Pro)
Xg.149482847G>ACA414517836IDSc.1552C>T (p.His518Tyr)
c.919C>T (p.His307Tyr)
c.1282C>T (p.His428Tyr)
Xg.149482847G>CCA10537433IDSc.1552C>G (p.His518Asp)
c.919C>G (p.His307Asp)
c.1282C>G (p.His428Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
Xg.149482847G=CA2465003951IDSc.1552C= (p.His518=)
c.919C= (p.His307=)
c.1282C= (p.His428=)
Xg.149482847G>TCA414517837IDSc.1552C>A (p.His518Asn)
c.919C>A (p.His307Asn)
c.1282C>A (p.His428Asn)
Xg.149482848G>ACA519057426IDSc.1551C>T (p.Ile517=)
c.918C>T (p.Ile306=)
c.1281C>T (p.Ile427=)
Xg.149482848G>CCA414517838IDSc.1551C>G (p.Ile517Met)
c.918C>G (p.Ile306Met)
c.1281C>G (p.Ile427Met)
Xg.149482848G>TCA519057424IDSc.1551C>A (p.Ile517=)
c.918C>A (p.Ile306=)
c.1281C>A (p.Ile427=)
Xg.149482849A>CCA414517839IDSc.1550T>G (p.Ile517Ser)
c.917T>G (p.Ile306Ser)
c.1280T>G (p.Ile427Ser)

Number of alleles fetched