Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.95101723A>GCA284829AOPEP,FANCCn.410+20943A>G
n.2476T>C
c.1661T>C (p.Leu554Pro)
c.1806T>C (n.1806T>C)
c.980T>C (p.Leu327Pro)
c.1496T>C (p.Leu499Pro)
c.1205T>C (p.Leu402Pro)
c.2319+20943A>G (n.2319+20943A>G)
c.1040T>C (p.Leu347Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.95101723A>CCA374104245AOPEP,FANCCn.410+20943A>C
n.2476T>G
c.1661T>G (p.Leu554Arg)
c.1806T>G (n.1806T>G)
c.980T>G (p.Leu327Arg)
c.1496T>G (p.Leu499Arg)
c.1205T>G (p.Leu402Arg)
c.2319+20943A>C (n.2319+20943A>C)
c.1040T>G (p.Leu347Arg)
dbSNP gnomAD v4
9g.95101723A=CA1865459507AOPEP,FANCCn.410+20943A=
n.2476T=
c.1661T= (p.Leu554=)
c.1806T= (n.1806T=)
c.980T= (p.Leu327=)
c.1496T= (p.Leu499=)
c.1205T= (p.Leu402=)
c.2319+20943A= (n.2319+20943A=)
c.1040T= (p.Leu347=)
dbSNP

Number of alleles fetched