Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.89919709C>A | CA286607471 | MC1R | c.451C>A (p.Arg151Ser) | dbSNP gnomAD v4 |
16 | g.89919709C>T | CA123871 | MC1R | c.451C>T (p.Arg151Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89919709C>G | CA286607469 | MC1R | c.451C>G (p.Arg151Gly) | dbSNP |
16 | g.89919709C= | CA2242009554 | MC1R | c.451C= (p.Arg151=) | dbSNP |