Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23415652G>A | CA015719 | MHRT,MYH7 | c.5134C>T (p.Arg1712Trp) n.84G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.23415652G= | CA2123463840 | MHRT,MYH7 | c.5134C= (p.Arg1712=) n.84G= | dbSNP |
14 | g.23415652G>C | CA389036894 | MHRT,MYH7 | c.5134C>G (p.Arg1712Gly) n.84G>C | dbSNP |