Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.47286294A>CCA400023435ITGB3c.649A>C (p.Lys217Gln)
c.614A>C
17g.47286294A>GCA400023436ITGB3c.649A>G (p.Lys217Glu)
c.614A>G
gnomAD v4
17g.47286294A>TCA400023437ITGB3c.649A>T (p.Lys217Ter)
c.614A>T
17g.47286295A>CCA400023438ITGB3c.650A>C (p.Lys217Thr)
c.615A>C
17g.47286295A>GCA400023439ITGB3c.650A>G (p.Lys217Arg)
c.615A>G
17g.47286295A>TCA400023440ITGB3c.650A>T (p.Lys217Ile)
c.615A>T
17g.47286296A=CA2262605985ITGB3c.651A= (p.Lys217=)
c.616A=
17g.47286296A>CCA400023441ITGB3c.651A>C (p.Lys217Asn)
c.616A>C
17g.47286296A>GCA500431969ITGB3c.651A>G (p.Lys217=)
c.616A>G
dbSNP gnomAD v3 gnomAD v4
17g.47286296A>TCA400023442ITGB3c.651A>T (p.Lys217Asn)
c.616A>T
gnomAD v4
17g.47286297C>ACA400023443ITGB3c.652C>A (p.His218Asn)
c.617C>A
17g.47286297C>GCA400023444ITGB3c.652C>G (p.His218Asp)
c.617C>G
17g.47286297C>TCA400023445ITGB3c.652C>T (p.His218Tyr)
c.617C>T
ClinVar dbSNP
17g.47286298A>CCA400023447ITGB3c.653A>C (p.His218Pro)
c.618A>C
17g.47286298A>GCA400023448ITGB3c.653A>G (p.His218Arg)
c.618A>G
gnomAD v4
17g.47286298A>TCA400023446ITGB3c.653A>T (p.His218Leu)
c.618A>T
17g.47286299C>ACA400023450ITGB3c.654C>A (p.His218Gln)
c.619C>A
17g.47286299C=CA2262605986ITGB3c.654C= (p.His218=)
c.619C=
17g.47286299C>GCA400023449ITGB3c.654C>G (p.His218Gln)
c.619C>G
17g.47286299C>TCA8623015ITGB3c.654C>T (p.His218=)
c.619C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286300G>ACA8623016ITGB3c.655G>A (p.Val219Met)
c.620G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.47286300G>CCA400023452ITGB3c.655G>C (p.Val219Leu)
c.620G>C
gnomAD v4
17g.47286300G=CA2262605987ITGB3c.655G= (p.Val219=)
c.620G=
17g.47286300G>TCA400023451ITGB3c.655G>T (p.Val219Leu)
c.620G>T
gnomAD v4
17g.47286301T>ACA400023453ITGB3c.656T>A (p.Val219Glu)
c.621T>A
17g.47286301T>CCA400023455ITGB3c.656T>C (p.Val219Ala)
c.621T>C
dbSNP gnomAD v3 gnomAD v4
17g.47286301T>GCA400023454ITGB3c.656T>G (p.Val219Gly)
c.621T>G
17g.47286301T=CA2262605988ITGB3c.656T= (p.Val219=)
c.621T=
17g.47286302G>ACA500431972ITGB3c.657G>A (p.Val219=)
c.622G>A
17g.47286302G>CCA500431971ITGB3c.657G>C (p.Val219=)
c.622G>C
gnomAD v4
17g.47286302G>TCA500431970ITGB3c.657G>T (p.Val219=)
c.622G>T
17g.47286303C>ACA400023456ITGB3c.658C>A (p.Leu220Met)
c.623C>A
17g.47286303C>GCA400023457ITGB3c.658C>G (p.Leu220Val)
c.623C>G
17g.47286303C>TCA500431973ITGB3c.658C>T (p.Leu220=)
c.623C>T
17g.47286304T>ACA400023458ITGB3c.659T>A (p.Leu220Gln)
c.624T>A
gnomAD v4
17g.47286304T>CCA400023459ITGB3c.659T>C (p.Leu220Pro)
c.624T>C
17g.47286304T>GCA400023460ITGB3c.659T>G (p.Leu220Arg)
c.624T>G
17g.47286305G>ACA500431975ITGB3c.660G>A (p.Leu220=)
c.625G>A
17g.47286305G>CCA500431974ITGB3c.660G>C (p.Leu220=)
c.625G>C
17g.47286305G>TCA500431976ITGB3c.660G>T (p.Leu220=)
c.625G>T
17g.47286306A>CCA400023461ITGB3c.661A>C (p.Thr221Pro)
c.626A>C
17g.47286306A>GCA400023462ITGB3c.661A>G (p.Thr221Ala)
c.626A>G
17g.47286306A>TCA400023463ITGB3c.661A>T (p.Thr221Ser)
c.626A>T
17g.47286307C>ACA400023464ITGB3c.662C>A (p.Thr221Lys)
c.627C>A
17g.47286307C=CA2262605989ITGB3c.662C= (p.Thr221=)
c.627C=
17g.47286307C>GCA400023465ITGB3c.662C>G (p.Thr221Arg)
c.627C>G
gnomAD v4
17g.47286307C>TCA8623017ITGB3c.662C>T (p.Thr221Met)
c.627C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286308G>ACA8623018ITGB3c.663G>A (p.Thr221=)
c.628G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47286308G>CCA500431977ITGB3c.663G>C (p.Thr221=)
c.628G>C
17g.47286308G=CA2262605990ITGB3c.663G= (p.Thr221=)
c.628G=

Number of alleles fetched