Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.75049586G>C | CA117588 | MLH3 | c.70C>G (p.Gln24Glu) n.286C>G n.233C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.75049586G>A | CA390451759 | MLH3 | c.70C>T (p.Gln24Ter) n.286C>T n.233C>T | ClinVar dbSNP |
14 | g.75049586G= | CA2147312458 | MLH3 | c.70C= (p.Gln24=) n.286C= n.233C= | dbSNP |