Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.124500585C>ACA467208185NR5A1c.375G>T (p.Pro125=)
c.40-313G>T (n.40-313G>T)
c.114G>T (p.Pro38=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.124500585C=CA1878469475NR5A1c.375G= (p.Pro125=)
c.40-313G= (n.40-313G=)
c.114G= (p.Pro38=)
9g.124500585C>GCA467208184NR5A1c.375G>C (p.Pro125=)
c.40-313G>C (n.40-313G>C)
c.114G>C (p.Pro38=)
9g.124500585C>TCA5235493NR5A1c.375G>A (p.Pro125=)
c.40-313G>A (n.40-313G>A)
c.114G>A (p.Pro38=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.124500586G>ACA5235495NR5A1c.374C>T (p.Pro125Leu)
c.40-314C>T (n.40-314C>T)
c.113C>T (p.Pro38Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.124500586G>CCA374888315NR5A1c.374C>G (p.Pro125Arg)
c.40-314C>G (n.40-314C>G)
c.113C>G (p.Pro38Arg)
9g.124500586G=CA1878469485NR5A1c.374C= (p.Pro125=)
c.40-314C= (n.40-314C=)
c.113C= (p.Pro38=)
9g.124500586G>TCA5235494NR5A1c.374C>A (p.Pro125Gln)
c.40-314C>A (n.40-314C>A)
c.113C>A (p.Pro38Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.124500586_124500587delinsAACA645548668NR5A1c.373_374delinsTT (p.Pro125Leu)
c.40-315_40-314delinsTT (n.40-315_40-314delinsTT)
c.112_113delinsTT (p.Pro38Leu)
COSMIC
9g.124500590dupCA590936671NR5A1c.374dup (p.Met126AspfsTer23)
c.40-314dup (n.40-314dup)
c.113dup (p.Met39AspfsTer23)
gnomAD v2
9g.124500590delCA2691611115NR5A1c.374del (p.Pro125ArgfsTer?)
c.40-314del (n.40-314del)
c.113del (p.Pro38ArgfsTer?)
gnomAD v4
9g.124500587G>ACA374888321NR5A1c.373C>T (p.Pro125Ser)
c.40-315C>T (n.40-315C>T)
c.112C>T (p.Pro38Ser)
dbSNP gnomAD v2
9g.124500587G>CCA374888323NR5A1c.373C>G (p.Pro125Ala)
c.40-315C>G (n.40-315C>G)
c.112C>G (p.Pro38Ala)
9g.124500587G=CA1878469492NR5A1c.373C= (p.Pro125=)
c.40-315C= (n.40-315C=)
c.112C= (p.Pro38=)
9g.124500587G>TCA374888325NR5A1c.373C>A (p.Pro125Thr)
c.40-315C>A (n.40-315C>A)
c.112C>A (p.Pro38Thr)
9g.124500588G>ACA467208190NR5A1c.372C>T (p.Pro124=)
c.40-316C>T (n.40-316C>T)
c.111C>T (p.Pro37=)
dbSNP gnomAD v3 gnomAD v4
9g.124500588G>CCA5235496NR5A1c.372C>G (p.Pro124=)
c.40-316C>G (n.40-316C>G)
c.111C>G (p.Pro37=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.124500588G=CA1878469495NR5A1c.372C= (p.Pro124=)
c.40-316C= (n.40-316C=)
c.111C= (p.Pro37=)
9g.124500588G>TCA467208188NR5A1c.372C>A (p.Pro124=)
c.40-316C>A (n.40-316C>A)
c.111C>A (p.Pro37=)
9g.124500589G>ACA374888339NR5A1c.371C>T (p.Pro124Leu)
c.40-317C>T (n.40-317C>T)
c.110C>T (p.Pro37Leu)
gnomAD v4
9g.124500589G>CCA374888336NR5A1c.371C>G (p.Pro124Arg)
c.40-317C>G (n.40-317C>G)
c.110C>G (p.Pro37Arg)
9g.124500589G=CA1878469499NR5A1c.371C= (p.Pro124=)
c.40-317C= (n.40-317C=)
c.110C= (p.Pro37=)
9g.124500589G>TCA374888333NR5A1c.371C>A (p.Pro124His)
c.40-317C>A (n.40-317C>A)
c.110C>A (p.Pro37His)
dbSNP gnomAD v4
9g.124500590G>ACA374888342NR5A1c.370C>T (p.Pro124Ser)
c.40-318C>T (n.40-318C>T)
c.109C>T (p.Pro37Ser)
dbSNP gnomAD v3 gnomAD v4
9g.124500590G>CCA5235497NR5A1c.370C>G (p.Pro124Ala)
c.40-318C>G (n.40-318C>G)
c.109C>G (p.Pro37Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.124500590G=CA1878469505NR5A1c.370C= (p.Pro124=)
c.40-318C= (n.40-318C=)
c.109C= (p.Pro37=)
9g.124500590G>TCA374888347NR5A1c.370C>A (p.Pro124Thr)
c.40-318C>A (n.40-318C>A)
c.109C>A (p.Pro37Thr)
9g.124500591C>ACA467208191NR5A1c.369G>T (p.Gly123=)
c.40-319G>T (n.40-319G>T)
c.108G>T (p.Gly36=)
dbSNP gnomAD v2 COSMIC
9g.124500591C=CA1878469508NR5A1c.369G= (p.Gly123=)
c.40-319G= (n.40-319G=)
c.108G= (p.Gly36=)
9g.124500591C>GCA467208193NR5A1c.369G>C (p.Gly123=)
c.40-319G>C (n.40-319G>C)
c.108G>C (p.Gly36=)
dbSNP
9g.124500591C>TCA467208192NR5A1c.369G>A (p.Gly123=)
c.40-319G>A (n.40-319G>A)
c.108G>A (p.Gly36=)
dbSNP gnomAD v2 gnomAD v4
9g.124500593delCA2695211097NR5A1c.369del (p.Pro125ArgfsTer?)
c.40-319del (n.40-319del)
c.108del (p.Pro38ArgfsTer?)
9g.124500593_124500600delCA2695211096NR5A1c.362_369del (p.Glu121AlafsTer25)
c.40-326_40-319del (n.40-326_40-319del)
c.101_108del (p.Glu34AlafsTer25)
9g.124500592C>ACA374888351NR5A1c.368G>T (p.Gly123Val)
c.40-320G>T (n.40-320G>T)
c.107G>T (p.Gly36Val)
9g.124500592C=CA1878469514NR5A1c.368G= (p.Gly123=)
c.40-320G= (n.40-320G=)
c.107G= (p.Gly36=)
9g.124500592C>GCA034488NR5A1c.368G>C (p.Gly123Ala)
c.40-320G>C (n.40-320G>C)
c.107G>C (p.Gly36Ala)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.124500592C>TCA374888355NR5A1c.368G>A (p.Gly123Glu)
c.40-320G>A (n.40-320G>A)
c.107G>A (p.Gly36Glu)
dbSNP gnomAD v2 gnomAD v4
9g.124500593C>ACA374888358NR5A1c.367G>T (p.Gly123Trp)
c.40-321G>T (n.40-321G>T)
c.106G>T (p.Gly36Trp)
9g.124500593C>GCA374888363NR5A1c.367G>C (p.Gly123Arg)
c.40-321G>C (n.40-321G>C)
c.106G>C (p.Gly36Arg)
9g.124500593C>TCA374888360NR5A1c.367G>A (p.Gly123Arg)
c.40-321G>A (n.40-321G>A)
c.106G>A (p.Gly36Arg)
9g.124500594T>ACA467208195NR5A1c.366A>T (p.Thr122=)
c.40-322A>T (n.40-322A>T)
c.105A>T (p.Thr35=)
9g.124500594T>CCA467208196NR5A1c.366A>G (p.Thr122=)
c.40-322A>G (n.40-322A>G)
c.105A>G (p.Thr35=)
dbSNP
9g.124500594T>GCA467208197NR5A1c.366A>C (p.Thr122=)
c.40-322A>C (n.40-322A>C)
c.105A>C (p.Thr35=)
9g.124500594T=CA1878469515NR5A1c.366A= (p.Thr122=)
c.40-322A= (n.40-322A=)
c.105A= (p.Thr35=)
9g.124500595G>ACA374888368NR5A1c.365C>T (p.Thr122Ile)
c.40-323C>T (n.40-323C>T)
c.104C>T (p.Thr35Ile)
9g.124500595G>CCA374888369NR5A1c.365C>G (p.Thr122Arg)
c.40-323C>G (n.40-323C>G)
c.104C>G (p.Thr35Arg)
9g.124500595G=CA1878469517NR5A1c.365C= (p.Thr122=)
c.40-323C= (n.40-323C=)
c.104C= (p.Thr35=)
9g.124500595G>TCA199729181NR5A1c.365C>A (p.Thr122Lys)
c.40-323C>A (n.40-323C>A)
c.104C>A (p.Thr35Lys)
dbSNP gnomAD v2 gnomAD v4
9g.124500596T>ACA374888374NR5A1c.364A>T (p.Thr122Ser)
c.40-324A>T (n.40-324A>T)
c.103A>T (p.Thr35Ser)
9g.124500596T>CCA374888376NR5A1c.364A>G (p.Thr122Ala)
c.40-324A>G (n.40-324A>G)
c.103A>G (p.Thr35Ala)
gnomAD v4

Number of alleles fetched