Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.122257265A>CCA354362752CASRc.370A>C (p.Asn124His)
c.9+2891A>C (p.=)
n.229A>C
3g.122257265A>GCA354362754CASRc.370A>G (p.Asn124Asp)
c.9+2891A>G (p.=)
n.229A>G
3g.122257265A>TCA354362753CASRc.370A>T (p.Asn124Tyr)
c.9+2891A>T (p.=)
n.229A>T
3g.122257266A>CCA354362755CASRc.371A>C (p.Asn124Thr)
c.9+2892A>C (p.=)
n.230A>C
3g.122257266A>GCA354362756CASRc.371A>G (p.Asn124Ser)
c.9+2892A>G (p.=)
n.230A>G
3g.122257266A>TCA354362757CASRc.371A>T (p.Asn124Ile)
c.9+2892A>T (p.=)
n.230A>T
3g.122257267C>ACA354362758CASRc.372C>A (p.Asn124Lys)
c.9+2893C>A (p.=)
n.231C>A
3g.122257267C>GCA354362759CASRc.372C>G (p.Asn124Lys)
c.9+2893C>G (p.=)
n.231C>G
3g.122257267C>TCA2569464CASRc.372C>T (p.Asn124=)
c.9+2893C>T (p.=)
n.231C>T
dbSNP ExAC gnomAD
3g.122257268C>ACA354362760CASRc.373C>A (p.Leu125Ile)
c.9+2894C>A (p.=)
n.232C>A
3g.122257268C>GCA354362761CASRc.373C>G (p.Leu125Val)
c.9+2894C>G (p.=)
n.232C>G
3g.122257268C>TCA354362762CASRc.373C>T (p.Leu125Phe)
c.9+2894C>T (p.=)
n.232C>T
3g.122257269T>ACA354362763CASRc.374T>A (p.Leu125His)
c.9+2895T>A (p.=)
n.233T>A
3g.122257269T>CCA119525CASRc.374T>C (p.Leu125Pro)
c.9+2895T>C (p.=)
n.233T>C
ClinVar dbSNP
3g.122257269T>GCA354362764CASRc.374T>G (p.Leu125Arg)
c.9+2895T>G (p.=)
n.233T>G
3g.122257270T>ACA435404096CASRc.375T>A (p.Leu125=)
c.9+2896T>A (p.=)
n.234T>A
3g.122257270T>CCA435404097CASRc.375T>C (p.Leu125=)
c.9+2896T>C (p.=)
n.234T>C
3g.122257270T>GCA2569465CASRc.375T>G (p.Leu125=)
c.9+2896T>G (p.=)
n.234T>G
ClinVar dbSNP ExAC
3g.122257271G>ACA354362767CASRc.376G>A (p.Asp126Asn)
c.9+2897G>A (p.=)
n.235G>A
3g.122257271G>CCA354362766CASRc.376G>C (p.Asp126His)
c.9+2897G>C (p.=)
n.235G>C
3g.122257271G>TCA354362765CASRc.376G>T (p.Asp126Tyr)
c.9+2897G>T (p.=)
n.235G>T
3g.122257272A>CCA354362768CASRc.377A>C (p.Asp126Ala)
c.9+2898A>C (p.=)
n.236A>C
3g.122257272A>GCA354362769CASRc.377A>G (p.Asp126Gly)
c.9+2898A>G (p.=)
n.236A>G
3g.122257272A>TCA354362770CASRc.377A>T (p.Asp126Val)
c.9+2898A>T (p.=)
n.236A>T
ClinVar
3g.122257273T>ACA354362771CASRc.378T>A (p.Asp126Glu)
c.9+2899T>A (p.=)
n.237T>A
3g.122257273T>CCA435404098CASRc.378T>C (p.Asp126=)
c.9+2899T>C (p.=)
n.237T>C
3g.122257273T>GCA354362772CASRc.378T>G (p.Asp126Glu)
c.9+2899T>G (p.=)
n.237T>G
3g.122257274G>ACA354362773CASRc.379G>A (p.Glu127Lys)
c.9+2900G>A (p.=)
n.238G>A
3g.122257274G>CCA354362774CASRc.379G>C (p.Glu127Gln)
c.9+2900G>C (p.=)
n.238G>C
3g.122257274G>TCA354362775CASRc.379G>T (p.Glu127Ter)
c.9+2900G>T (p.=)
n.238G>T
3g.122257275A>CCA119473CASRc.380A>C (p.Glu127Ala)
c.9+2901A>C (p.=)
n.239A>C
ClinVar dbSNP
3g.122257275A>GCA213599CASRc.380A>G (p.Glu127Gly)
c.9+2901A>G (p.=)
n.239A>G
ClinVar dbSNP
3g.122257275A>TCA354362776CASRc.380A>T (p.Glu127Val)
c.9+2901A>T (p.=)
n.239A>T
3g.122257276G>ACA435404099CASRc.381G>A (p.Glu127=)
c.9+2902G>A (p.=)
n.240G>A
3g.122257276G>CCA354362777CASRc.381G>C (p.Glu127Asp)
c.9+2902G>C (p.=)
n.240G>C
3g.122257276G>TCA354362778CASRc.381G>T (p.Glu127Asp)
c.9+2902G>T (p.=)
n.240G>T
3g.122257277T>ACA354362780CASRc.382T>A (p.Phe128Ile)
c.9+2903T>A (p.=)
n.241T>A
3g.122257277T>CCA119489CASRc.382T>C (p.Phe128Leu)
c.9+2903T>C (p.=)
n.241T>C
ClinVar dbSNP COSMIC
3g.122257277T>GCA354362779CASRc.382T>G (p.Phe128Val)
c.9+2903T>G (p.=)
n.241T>G
3g.122257278T>ACA354362781CASRc.383T>A (p.Phe128Tyr)
c.9+2904T>A (p.=)
n.242T>A
3g.122257278T>CCA354362782CASRc.383T>C (p.Phe128Ser)
c.9+2904T>C (p.=)
n.242T>C
3g.122257278T>GCA354362783CASRc.383T>G (p.Phe128Cys)
c.9+2904T>G (p.=)
n.242T>G
3g.122257279C>ACA354362784CASRc.384C>A (p.Phe128Leu)
c.9+2905C>A (p.=)
n.243C>A
ClinVar
3g.122257279C>GCA354362785CASRc.384C>G (p.Phe128Leu)
c.9+2905C>G (p.=)
n.243C>G
3g.122257279C>TCA435404100CASRc.384C>T (p.Phe128=)
c.9+2905C>T (p.=)
n.243C>T
3g.122257280T>ACA354362786CASRc.385T>A (p.Cys129Ser)
c.9+2906T>A (p.=)
n.244T>A
3g.122257280T>CCA354362787CASRc.385T>C (p.Cys129Arg)
c.9+2906T>C (p.=)
n.244T>C
3g.122257280T>GCA354362788CASRc.385T>G (p.Cys129Gly)
c.9+2906T>G (p.=)
n.244T>G
3g.122257281G>ACA354362789CASRc.386G>A (p.Cys129Tyr)
c.9+2907G>A (p.=)
n.245G>A
3g.122257281G>CCA354362790CASRc.386G>C (p.Cys129Ser)
c.9+2907G>C (p.=)
n.245G>C

Number of alleles fetched