Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.52451410G>T | CA122401 | TNNC1 | c.435C>A (p.Asp145Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.52451410G>C | CA2438493 | TNNC1 | c.435C>G (p.Asp145Glu) | dbSNP ExAC gnomAD v2 |
3 | g.52451410G>A | CA2438492 | TNNC1 | c.435C>T (p.Asp145=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |