Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.6277628C>ACA356169778WFS1n.343C>A
c.173C>A (p.Ala58Glu)
c.163C>A
c.-18+7614C>A (n.-18+7614C>A)
c.67-20C>A (n.67-20C>A)
c.182C>A (p.Ala61Glu)
dbSNP gnomAD v4
4g.6277628C=CA1435762671WFS1n.343C=
c.173C= (p.Ala58=)
c.163C=
c.-18+7614C= (n.-18+7614C=)
c.67-20C= (n.67-20C=)
c.182C= (p.Ala61=)
4g.6277628C>GCA356169777WFS1n.343C>G
c.173C>G (p.Ala58Gly)
c.163C>G
c.-18+7614C>G (n.-18+7614C>G)
c.67-20C>G (n.67-20C>G)
c.182C>G (p.Ala61Gly)
4g.6277628C>TCA2838811WFS1n.343C>T
c.173C>T (p.Ala58Val)
c.163C>T
c.-18+7614C>T (n.-18+7614C>T)
c.67-20C>T (n.67-20C>T)
c.182C>T (p.Ala61Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6277629G>ACA438210571WFS1n.344G>A
c.174G>A (p.Ala58=)
c.164G>A
c.-18+7615G>A (n.-18+7615G>A)
c.67-19G>A (n.67-19G>A)
c.183G>A (p.Ala61=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6277629G>CCA438210572WFS1n.344G>C
c.174G>C (p.Ala58=)
c.164G>C
c.-18+7615G>C (n.-18+7615G>C)
c.67-19G>C (n.67-19G>C)
c.183G>C (p.Ala61=)
4g.6277629G=CA1435762678WFS1n.344G=
c.174G= (p.Ala58=)
c.164G=
c.-18+7615G= (n.-18+7615G=)
c.67-19G= (n.67-19G=)
c.183G= (p.Ala61=)
4g.6277629G>TCA438210573WFS1n.344G>T
c.174G>T (p.Ala58=)
c.164G>T
c.-18+7615G>T (n.-18+7615G>T)
c.67-19G>T (n.67-19G>T)
c.183G>T (p.Ala61=)
4g.6277630delCA2586973591WFS1n.345del
c.175del (p.Ala59ProfsTer?)
c.165del
c.-18+7616del (n.-18+7616del)
c.67-18del (n.67-18del)
c.184del (p.Ala62ProfsTer?)
4g.6277630G>ACA91787498WFS1n.345G>A
c.175G>A (p.Ala59Thr)
c.165G>A
c.-18+7616G>A (n.-18+7616G>A)
c.67-18G>A (n.67-18G>A)
c.184G>A (p.Ala62Thr)
dbSNP gnomAD v2 gnomAD v4
4g.6277630G>CCA356169779WFS1n.345G>C
c.175G>C (p.Ala59Pro)
c.165G>C
c.-18+7616G>C (n.-18+7616G>C)
c.67-18G>C (n.67-18G>C)
c.184G>C (p.Ala62Pro)
4g.6277630G=CA1435762680WFS1n.345G=
c.175G= (p.Ala59=)
c.165G=
c.-18+7616G= (n.-18+7616G=)
c.67-18G= (n.67-18G=)
c.184G= (p.Ala62=)
4g.6277630G>TCA356169780WFS1n.345G>T
c.175G>T (p.Ala59Ser)
c.165G>T
c.-18+7616G>T (n.-18+7616G>T)
c.67-18G>T (n.67-18G>T)
c.184G>T (p.Ala62Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6277631C>ACA356169782WFS1n.346C>A
c.176C>A (p.Ala59Asp)
c.166C>A
c.-18+7617C>A (n.-18+7617C>A)
c.67-17C>A (n.67-17C>A)
c.185C>A (p.Ala62Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6277631C=CA1435762687WFS1n.346C=
c.176C= (p.Ala59=)
c.166C=
c.-18+7617C= (n.-18+7617C=)
c.67-17C= (n.67-17C=)
c.185C= (p.Ala62=)
4g.6277631C>GCA356169781WFS1n.346C>G
c.176C>G (p.Ala59Gly)
c.166C>G
c.-18+7617C>G (n.-18+7617C>G)
c.67-17C>G (n.67-17C>G)
c.185C>G (p.Ala62Gly)
4g.6277631C>TCA2838812WFS1n.346C>T
c.176C>T (p.Ala59Val)
c.166C>T
c.-18+7617C>T (n.-18+7617C>T)
c.67-17C>T (n.67-17C>T)
c.185C>T (p.Ala62Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6277635delCA2669824813WFS1n.350del
c.180del (p.Ala61LeufsTer?)
c.170del
c.-18+7621del (n.-18+7621del)
c.67-13del (n.67-13del)
c.189del (p.Ala64LeufsTer?)
gnomAD v4
4g.6277632C>ACA438210576WFS1n.347C>A
c.177C>A (p.Ala59=)
c.167C>A
c.-18+7618C>A (n.-18+7618C>A)
c.67-16C>A (n.67-16C>A)
c.186C>A (p.Ala62=)
4g.6277632C=CA1435762693WFS1n.347C=
c.177C= (p.Ala59=)
c.167C=
c.-18+7618C= (n.-18+7618C=)
c.67-16C= (n.67-16C=)
c.186C= (p.Ala62=)
4g.6277632C>GCA438210575WFS1n.347C>G
c.177C>G (p.Ala59=)
c.167C>G
c.-18+7618C>G (n.-18+7618C>G)
c.67-16C>G (n.67-16C>G)
c.186C>G (p.Ala62=)
gnomAD v4
4g.6277632C>TCA438210574WFS1n.347C>T
c.177C>T (p.Ala59=)
c.167C>T
c.-18+7618C>T (n.-18+7618C>T)
c.67-16C>T (n.67-16C>T)
c.186C>T (p.Ala62=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6277633C>ACA356169783WFS1n.348C>A
c.178C>A (p.Pro60Thr)
c.168C>A
c.-18+7619C>A (n.-18+7619C>A)
c.67-15C>A (n.67-15C>A)
c.187C>A (p.Pro63Thr)
gnomAD v4
4g.6277633C>GCA356169784WFS1n.348C>G
c.178C>G (p.Pro60Ala)
c.168C>G
c.-18+7619C>G (n.-18+7619C>G)
c.67-15C>G (n.67-15C>G)
c.187C>G (p.Pro63Ala)
gnomAD v4
4g.6277633C>TCA356169785WFS1n.348C>T
c.178C>T (p.Pro60Ser)
c.168C>T
c.-18+7619C>T (n.-18+7619C>T)
c.67-15C>T (n.67-15C>T)
c.187C>T (p.Pro63Ser)
gnomAD v4
4g.6277634C>ACA356169786WFS1n.349C>A
c.179C>A (p.Pro60His)
c.169C>A
c.-18+7620C>A (n.-18+7620C>A)
c.67-14C>A (n.67-14C>A)
c.188C>A (p.Pro63His)
gnomAD v4
4g.6277634C>GCA356169787WFS1n.349C>G
c.179C>G (p.Pro60Arg)
c.169C>G
c.-18+7620C>G (n.-18+7620C>G)
c.67-14C>G (n.67-14C>G)
c.188C>G (p.Pro63Arg)
4g.6277634C>TCA356169788WFS1n.349C>T
c.179C>T (p.Pro60Leu)
c.169C>T
c.-18+7620C>T (n.-18+7620C>T)
c.67-14C>T (n.67-14C>T)
c.188C>T (p.Pro63Leu)
gnomAD v4
4g.6277635C>ACA438210578WFS1n.350C>A
c.180C>A (p.Pro60=)
c.170C>A
c.-18+7621C>A (n.-18+7621C>A)
c.67-13C>A (n.67-13C>A)
c.189C>A (p.Pro63=)
gnomAD v4
4g.6277635C=CA1435762694WFS1n.350C=
c.180C= (p.Pro60=)
c.170C=
c.-18+7621C= (n.-18+7621C=)
c.67-13C= (n.67-13C=)
c.189C= (p.Pro63=)
4g.6277635C>GCA438210579WFS1n.350C>G
c.180C>G (p.Pro60=)
c.170C>G
c.-18+7621C>G (n.-18+7621C>G)
c.67-13C>G (n.67-13C>G)
c.189C>G (p.Pro63=)
4g.6277635C>TCA438210580WFS1n.350C>T
c.180C>T (p.Pro60=)
c.170C>T
c.-18+7621C>T (n.-18+7621C>T)
c.67-13C>T (n.67-13C>T)
c.189C>T (p.Pro63=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6277636G>ACA2838814WFS1n.351G>A
c.181G>A (p.Ala61Thr)
c.171G>A
c.-18+7622G>A (n.-18+7622G>A)
c.67-12G>A (n.67-12G>A)
c.190G>A (p.Ala64Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6277636G>CCA356169789WFS1n.351G>C
c.181G>C (p.Ala61Pro)
c.171G>C
c.-18+7622G>C (n.-18+7622G>C)
c.67-12G>C (n.67-12G>C)
c.190G>C (p.Ala64Pro)
4g.6277636G=CA1435762699WFS1n.351G=
c.181G= (p.Ala61=)
c.171G=
c.-18+7622G= (n.-18+7622G=)
c.67-12G= (n.67-12G=)
c.190G= (p.Ala64=)
4g.6277636G>TCA2838813WFS1n.351G>T
c.181G>T (p.Ala61Ser)
c.171G>T
c.-18+7622G>T (n.-18+7622G>T)
c.67-12G>T (n.67-12G>T)
c.190G>T (p.Ala64Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.6277637C>ACA356169790WFS1n.352C>A
c.182C>A (p.Ala61Asp)
c.172C>A
c.-18+7623C>A (n.-18+7623C>A)
c.67-11C>A (n.67-11C>A)
c.191C>A (p.Ala64Asp)
gnomAD v4
4g.6277637C>GCA356169791WFS1n.352C>G
c.182C>G (p.Ala61Gly)
c.172C>G
c.-18+7623C>G (n.-18+7623C>G)
c.67-11C>G (n.67-11C>G)
c.191C>G (p.Ala64Gly)
4g.6277637C>TCA356169792WFS1n.352C>T
c.182C>T (p.Ala61Val)
c.172C>T
c.-18+7623C>T (n.-18+7623C>T)
c.67-11C>T (n.67-11C>T)
c.191C>T (p.Ala64Val)
gnomAD v4
4g.6277638T>ACA438210584WFS1n.353T>A
c.183T>A (p.Ala61=)
c.173T>A
c.-18+7624T>A (n.-18+7624T>A)
c.67-10T>A (n.67-10T>A)
c.192T>A (p.Ala64=)
4g.6277638T>CCA438210583WFS1n.353T>C
c.183T>C (p.Ala61=)
c.173T>C
c.-18+7624T>C (n.-18+7624T>C)
c.67-10T>C (n.67-10T>C)
c.192T>C (p.Ala64=)
dbSNP gnomAD v3 gnomAD v4
4g.6277638T>GCA438210582WFS1n.353T>G
c.183T>G (p.Ala61=)
c.173T>G
c.-18+7624T>G (n.-18+7624T>G)
c.67-10T>G (n.67-10T>G)
c.192T>G (p.Ala64=)
dbSNP gnomAD v2 gnomAD v4
4g.6277638T=CA1435762705WFS1n.353T=
c.183T= (p.Ala61=)
c.173T=
c.-18+7624T= (n.-18+7624T=)
c.67-10T= (n.67-10T=)
c.192T= (p.Ala64=)
4g.6277639G>ACA356169793WFS1n.354G>A
c.184G>A (p.Glu62Lys)
c.174G>A
c.-18+7625G>A (n.-18+7625G>A)
c.67-9G>A (n.67-9G>A)
c.193G>A (p.Glu65Lys)
gnomAD v4 COSMIC
4g.6277639G>CCA356169794WFS1n.354G>C
c.184G>C (p.Glu62Gln)
c.174G>C
c.-18+7625G>C (n.-18+7625G>C)
c.67-9G>C (n.67-9G>C)
c.193G>C (p.Glu65Gln)
4g.6277639G>TCA356169795WFS1n.354G>T
c.184G>T (p.Glu62Ter)
c.174G>T
c.-18+7625G>T (n.-18+7625G>T)
c.67-9G>T (n.67-9G>T)
c.193G>T (p.Glu65Ter)
gnomAD v4
4g.6277640A>CCA356169796WFS1n.355A>C
c.185A>C (p.Glu62Ala)
c.175A>C
c.-18+7626A>C (n.-18+7626A>C)
c.67-8A>C (n.67-8A>C)
c.194A>C (p.Glu65Ala)
4g.6277640A>GCA356169797WFS1n.355A>G
c.185A>G (p.Glu62Gly)
c.175A>G
c.-18+7626A>G (n.-18+7626A>G)
c.67-8A>G (n.67-8A>G)
c.194A>G (p.Glu65Gly)
4g.6277640A>TCA356169798WFS1n.355A>T
c.185A>T (p.Glu62Val)
c.175A>T
c.-18+7626A>T (n.-18+7626A>T)
c.67-8A>T (n.67-8A>T)
c.194A>T (p.Glu65Val)
4g.6277641A>CCA356169799WFS1n.356A>C
c.186A>C (p.Glu62Asp)
c.176A>C
c.-18+7627A>C (n.-18+7627A>C)
c.67-7A>C (n.67-7A>C)
c.195A>C (p.Glu65Asp)

Number of alleles fetched