Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.75047435C>A | CA117594 | MLH3 | c.2221G>T (p.Val741Phe) n.2437G>T n.2384G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.75047435C>T | CA7275733 | MLH3 | c.2221G>A (p.Val741Ile) n.2437G>A n.2384G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |