Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.23417295C>A | CA014901 | MHRT,MYH7 | c.4377G>T (p.Lys1459Asn) n.735C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.23417295C>T | CA042099 | MHRT,MYH7 | c.4377G>A (p.Lys1459=) n.735C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.23417295C>G | CA389038810 | MHRT,MYH7 | c.4377G>C (p.Lys1459Asn) n.735C>G | dbSNP gnomAD v4 |