Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.49451591G>C | CA3846942 | MMUT | c.1207C>G (p.Arg403Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49451591G>A | CA234287 | MMUT | c.1207C>T (p.Arg403Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.49451591G= | CA1627389333 | MMUT | c.1207C= (p.Arg403=) | dbSNP |
6 | g.49451591G>T | CA450606476 | MMUT | c.1207C>A (p.Arg403=) | dbSNP gnomAD v4 |