Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23417173C>A | CA257811620 | MHRT,MYH7 | c.4499G>T (p.Arg1500Leu) n.652-39C>A | dbSNP |
14 | g.23417173C>T | CA015036 | MHRT,MYH7 | c.4499G>A (p.Arg1500Gln) n.652-39C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
14 | g.23417173C>G | CA015044 | MHRT,MYH7 | c.4499G>C (p.Arg1500Pro) n.652-39C>G | ClinVar dbSNP |