Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.122257259T>ACA354362739CASRc.364T>A (p.Ser122Thr)
c.9+2885T>A (p.=)
n.223T>A
3g.122257259T>CCA354362741CASRc.364T>C (p.Ser122Pro)
c.9+2885T>C (p.=)
n.223T>C
3g.122257259T>GCA354362742CASRc.364T>G (p.Ser122Ala)
c.9+2885T>G (p.=)
n.223T>G
3g.122257260C>ACA2569462CASRc.365C>A (p.Ser122Tyr)
c.9+2886C>A (p.=)
n.224C>A
ClinVar dbSNP ExAC gnomAD COSMIC
3g.122257260C>GCA354362743CASRc.365C>G (p.Ser122Cys)
c.9+2886C>G (p.=)
n.224C>G
3g.122257260C>TCA354362744CASRc.365C>T (p.Ser122Phe)
c.9+2886C>T (p.=)
n.224C>T
3g.122257261T>ACA435404091CASRc.366T>A (p.Ser122=)
c.9+2887T>A (p.=)
n.225T>A
3g.122257261T>CCA435404092CASRc.366T>C (p.Ser122=)
c.9+2887T>C (p.=)
n.225T>C
3g.122257261T>GCA2569463CASRc.366T>G (p.Ser122=)
c.9+2887T>G (p.=)
n.225T>G
dbSNP ExAC gnomAD
3g.122257262T>ACA354362745CASRc.367T>A (p.Leu123Met)
c.9+2888T>A (p.=)
n.226T>A
3g.122257262T>CCA435404093CASRc.367T>C (p.Leu123=)
c.9+2888T>C (p.=)
n.226T>C
3g.122257262T>GCA354362746CASRc.367T>G (p.Leu123Val)
c.9+2888T>G (p.=)
n.226T>G
3g.122257263T>ACA354362747CASRc.368T>A (p.Leu123Ter)
c.9+2889T>A (p.=)
n.227T>A
3g.122257263T>CCA354362748CASRc.368T>C (p.Leu123Ser)
c.9+2889T>C (p.=)
n.227T>C
3g.122257263T>GCA354362749CASRc.368T>G (p.Leu123Trp)
c.9+2889T>G (p.=)
n.227T>G
3g.122257264G>ACA435404095CASRc.369G>A (p.Leu123=)
c.9+2890G>A (p.=)
n.228G>A
3g.122257264G>CCA354362751CASRc.369G>C (p.Leu123Phe)
c.9+2890G>C (p.=)
n.228G>C
3g.122257264G>TCA354362750CASRc.369G>T (p.Leu123Phe)
c.9+2890G>T (p.=)
n.228G>T
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

Number of alleles fetched