Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.894156C>TCA4961650DMRT1c.783C>T (p.Pro261=)
n.932C>T
c.309C>T (p.Pro103=)
c.831C>T (p.Pro277=)
c.587-22607C>T (n.587-22607C>T)
c.539-22607C>T (n.539-22607C>T)
c.237C>T (p.Pro79=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.894156C>GCA4961651DMRT1c.783C>G (p.Pro261=)
n.932C>G
c.309C>G (p.Pro103=)
c.831C>G (p.Pro277=)
c.587-22607C>G (n.587-22607C>G)
c.539-22607C>G (n.539-22607C>G)
c.237C>G (p.Pro79=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched