Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.51915293G>T | CA16613819 | ACVRL1 | c.571G>T (p.Glu191Ter) c.841G>T (p.Glu281Ter) c.319G>T (p.Glu107Ter) c.883G>T (p.Glu295Ter) c.52G>T (p.Glu18Ter) | ClinVar dbSNP gnomAD v4 |
12 | g.51915293G>C | CA384900515 | ACVRL1 | c.571G>C (p.Glu191Gln) c.841G>C (p.Glu281Gln) c.319G>C (p.Glu107Gln) c.883G>C (p.Glu295Gln) c.52G>C (p.Glu18Gln) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.51915293G>A | CA6573006 | ACVRL1 | c.571G>A (p.Glu191Lys) c.841G>A (p.Glu281Lys) c.319G>A (p.Glu107Lys) c.883G>A (p.Glu295Lys) c.52G>A (p.Glu18Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |