Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.75047180T>C | CA7275698 | MLH3 | c.2476A>G (p.Asn826Asp) n.22A>G n.2692A>G n.2639A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.75047180T>G | CA390440282 | MLH3 | c.2476A>C (p.Asn826His) n.22A>C n.2692A>C n.2639A>C | dbSNP |
14 | g.75047180T>A | CA390440279 | MLH3 | c.2476A>T (p.Asn826Tyr) n.22A>T n.2692A>T n.2639A>T | dbSNP gnomAD v4 |