Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.229432568C>G | CA10602749 | ACTA1 | c.442G>C (p.Gly148Arg) c.307G>C (p.Gly103Arg) | ClinVar dbSNP |
1 | g.229432568C>T | CA221485 | ACTA1 | c.442G>A (p.Gly148Ser) c.307G>A (p.Gly103Ser) | ClinVar dbSNP |
1 | g.229432568C= | CA1144233516 | ACTA1 | c.442G= (p.Gly148=) c.307G= (p.Gly103=) | dbSNP |