Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.49473613T>CCA274704ERCC6c.2599-26A>G (p.=)
c.*895-26A>G (p.=)
c.709-26A>G (p.=)
n.431-26A>G
ClinVar dbSNP ExAC gnomAD
10g.49473613T>GCA206587510ERCC6c.2599-26A>C (p.=)
c.*895-26A>C (p.=)
c.709-26A>C (p.=)
n.431-26A>C
dbSNP gnomAD

Number of alleles fetched