Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.229432867C>A | CA345151023 | ACTA1 | c.143G>T (p.Gly48Val) c.8G>T (p.Gly3Val) | ClinVar dbSNP |
1 | g.229432867C>T | CA344554 | ACTA1 | c.143G>A (p.Gly48Asp) c.8G>A (p.Gly3Asp) | ClinVar dbSNP |
1 | g.229432867C>G | CA345151024 | ACTA1 | c.143G>C (p.Gly48Ala) c.8G>C (p.Gly3Ala) | ClinVar dbSNP |
1 | g.229432867C= | CA1143538620 | ACTA1 | c.143G= (p.Gly48=) c.8G= (p.Gly3=) | dbSNP |