Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23424893A>G | CA012623 | MYH7 | c.2555T>C (p.Met852Thr) n.2661T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23424893A>T | CA012614 | MYH7 | c.2555T>A (p.Met852Lys) n.2661T>A | ClinVar dbSNP |
14 | g.23424893A>C | CA389048167 | MYH7 | c.2555T>G (p.Met852Arg) n.2661T>G | ClinVar dbSNP |