Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.52453993G>C | CA353170797 | TNNC1 | c.23C>G (p.Ala8Gly) | ClinVar dbSNP |
3 | g.52453993G>A | CA122397 | TNNC1 | c.23C>T (p.Ala8Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.52453993G= | CA1364864855 | TNNC1 | c.23C= (p.Ala8=) | dbSNP |
3 | g.52453993G>T | CA353170798 | TNNC1 | c.23C>A (p.Ala8Glu) | dbSNP gnomAD v4 |