Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.10394341A>G | CA153830 | MYH8,MYHAS | c.5074T>C (p.Trp1692Arg) n.76+11134A>G c.5170T>C (p.Trp1724Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.10394341A>T | CA398094961 | MYH8,MYHAS | c.5074T>A (p.Trp1692Arg) n.76+11134A>T c.5170T>A (p.Trp1724Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |