Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.189575196A>CCA349989671SLC40A1c.236T>G (p.Ile79Ser)
n.677T>G
n.517T>G
c.116T>G (p.Ile39Ser)
2g.189575196A>GCA349989672SLC40A1c.236T>C (p.Ile79Thr)
n.677T>C
n.517T>C
c.116T>C (p.Ile39Thr)
2g.189575196A>TCA349989673SLC40A1c.236T>A (p.Ile79Asn)
n.677T>A
n.517T>A
c.116T>A (p.Ile39Asn)
2g.189575197T>ACA349989676SLC40A1c.235A>T (p.Ile79Phe)
n.676A>T
n.516A>T
c.115A>T (p.Ile39Phe)
2g.189575197T>CCA349989674SLC40A1c.235A>G (p.Ile79Val)
n.676A>G
n.516A>G
c.115A>G (p.Ile39Val)
ClinVar dbSNP gnomAD v4
2g.189575197T>GCA349989675SLC40A1c.235A>C (p.Ile79Leu)
n.676A>C
n.516A>C
c.115A>C (p.Ile39Leu)
2g.189575197T=CA1315653679SLC40A1c.235A= (p.Ile79=)
n.676A=
n.516A=
c.115A= (p.Ile39=)
2g.189575198G>ACA430367503SLC40A1c.234C>T (p.Ile78=)
n.675C>T
n.515C>T
c.114C>T (p.Ile38=)
dbSNP
2g.189575198G>CCA349989677SLC40A1c.234C>G (p.Ile78Met)
n.675C>G
n.515C>G
c.114C>G (p.Ile38Met)
2g.189575198G=CA1315653684SLC40A1c.234C= (p.Ile78=)
n.675C=
n.515C=
c.114C= (p.Ile38=)
2g.189575198G>TCA430367504SLC40A1c.234C>A (p.Ile78=)
n.675C>A
n.515C>A
c.114C>A (p.Ile38=)
2g.189575199A>CCA349989678SLC40A1c.233T>G (p.Ile78Ser)
n.674T>G
n.514T>G
c.113T>G (p.Ile38Ser)
2g.189575199A>GCA349989679SLC40A1c.233T>C (p.Ile78Thr)
n.674T>C
n.514T>C
c.113T>C (p.Ile38Thr)
2g.189575199A>TCA349989680SLC40A1c.233T>A (p.Ile78Asn)
n.674T>A
n.514T>A
c.113T>A (p.Ile38Asn)
2g.189575200T>ACA349989681SLC40A1c.232A>T (p.Ile78Phe)
n.673A>T
n.513A>T
c.112A>T (p.Ile38Phe)
2g.189575200T>CCA349989682SLC40A1c.232A>G (p.Ile78Val)
n.673A>G
n.513A>G
c.112A>G (p.Ile38Val)
gnomAD v4
2g.189575200T>GCA349989683SLC40A1c.232A>C (p.Ile78Leu)
n.673A>C
n.513A>C
c.112A>C (p.Ile38Leu)
2g.189575201G>ACA430367505SLC40A1c.231C>T (p.Ala77=)
n.672C>T
n.512C>T
c.111C>T (p.Ala37=)
2g.189575201G>CCA430367506SLC40A1c.231C>G (p.Ala77=)
n.672C>G
n.512C>G
c.111C>G (p.Ala37=)
2g.189575201G>TCA430367507SLC40A1c.231C>A (p.Ala77=)
n.672C>A
n.512C>A
c.111C>A (p.Ala37=)
2g.189575202G>ACA349989684SLC40A1c.230C>T (p.Ala77Val)
n.671C>T
n.511C>T
c.110C>T (p.Ala37Val)
2g.189575202G>CCA349989685SLC40A1c.230C>G (p.Ala77Gly)
n.671C>G
n.511C>G
c.110C>G (p.Ala37Gly)
COSMIC
2g.189575202G=CA1315653689SLC40A1c.230C= (p.Ala77=)
n.671C=
n.511C=
c.110C= (p.Ala37=)
2g.189575202G>TCA117517SLC40A1c.230C>A (p.Ala77Asp)
n.671C>A
n.511C>A
c.110C>A (p.Ala37Asp)
ClinVar dbSNP
2g.189575203C>ACA349989686SLC40A1c.229G>T (p.Ala77Ser)
n.670G>T
n.510G>T
c.109G>T (p.Ala37Ser)
2g.189575203C=CA1315653694SLC40A1c.229G= (p.Ala77=)
n.670G=
n.510G=
c.109G= (p.Ala37=)
2g.189575203C>GCA349989687SLC40A1c.229G>C (p.Ala77Pro)
n.670G>C
n.510G>C
c.109G>C (p.Ala37Pro)
2g.189575203C>TCA62904036SLC40A1c.229G>A (p.Ala77Thr)
n.670G>A
n.510G>A
c.109G>A (p.Ala37Thr)
dbSNP
2g.189575204T>ACA430367508SLC40A1c.228A>T (p.Gly76=)
n.669A>T
n.509A>T
c.108A>T (p.Gly36=)
2g.189575204T>CCA430367509SLC40A1c.228A>G (p.Gly76=)
n.669A>G
n.509A>G
c.108A>G (p.Gly36=)
dbSNP gnomAD v2 gnomAD v4
2g.189575204T>GCA430367510SLC40A1c.228A>C (p.Gly76=)
n.669A>C
n.509A>C
c.108A>C (p.Gly36=)
2g.189575204T=CA1315653696SLC40A1c.228A= (p.Gly76=)
n.669A=
n.509A=
c.108A= (p.Gly36=)
2g.189575205C>ACA349989690SLC40A1c.227G>T (p.Gly76Val)
n.668G>T
n.508G>T
c.107G>T (p.Gly36Val)
2g.189575205C>GCA349989689SLC40A1c.227G>C (p.Gly76Ala)
n.668G>C
n.508G>C
c.107G>C (p.Gly36Ala)
2g.189575205C>TCA349989688SLC40A1c.227G>A (p.Gly76Glu)
n.668G>A
n.508G>A
c.107G>A (p.Gly36Glu)
COSMIC
2g.189575206C>ACA349989691SLC40A1c.226G>T (p.Gly76Ter)
n.667G>T
n.507G>T
c.106G>T (p.Gly36Ter)
2g.189575206C>GCA349989692SLC40A1c.226G>C (p.Gly76Arg)
n.667G>C
n.507G>C
c.106G>C (p.Gly36Arg)
2g.189575206C>TCA349989693SLC40A1c.226G>A (p.Gly76Arg)
n.667G>A
n.507G>A
c.106G>A (p.Gly36Arg)
2g.189575207C>ACA430367511SLC40A1c.225G>T (p.Leu75=)
n.666G>T
n.506G>T
c.105G>T (p.Leu35=)
2g.189575207C>GCA430367512SLC40A1c.225G>C (p.Leu75=)
n.666G>C
n.506G>C
c.105G>C (p.Leu35=)
COSMIC
2g.189575207C>TCA430367513SLC40A1c.225G>A (p.Leu75=)
n.666G>A
n.506G>A
c.105G>A (p.Leu35=)
2g.189575208A=CA1315653699SLC40A1c.224T= (p.Leu75=)
n.665T=
n.505T=
c.104T= (p.Leu35=)
2g.189575208A>CCA349989694SLC40A1c.224T>G (p.Leu75Arg)
n.665T>G
n.505T>G
c.104T>G (p.Leu35Arg)
2g.189575208A>GCA62904037SLC40A1c.224T>C (p.Leu75Pro)
n.665T>C
n.505T>C
c.104T>C (p.Leu35Pro)
dbSNP
2g.189575208A>TCA349989695SLC40A1c.224T>A (p.Leu75Gln)
n.665T>A
n.505T>A
c.104T>A (p.Leu35Gln)
2g.189575209G>ACA430367514SLC40A1c.223C>T (p.Leu75=)
n.664C>T
n.504C>T
c.103C>T (p.Leu35=)
2g.189575209G>CCA349989696SLC40A1c.223C>G (p.Leu75Val)
n.664C>G
n.504C>G
c.103C>G (p.Leu35Val)
COSMIC
2g.189575209G>TCA349989697SLC40A1c.223C>A (p.Leu75Met)
n.664C>A
n.504C>A
c.103C>A (p.Leu35Met)
2g.189575210G>ACA430367515SLC40A1c.222C>T (p.Val74=)
n.663C>T
n.503C>T
c.102C>T (p.Val34=)
2g.189575210G>CCA430367516SLC40A1c.222C>G (p.Val74=)
n.663C>G
n.503C>G
c.102C>G (p.Val34=)

Number of alleles fetched