Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.95155662A>T | CA1477970727 | BMPR1B | c.*989A>T (n.*989A>T) c.*13+976A>T (n.*13+976A>T) | dbSNP |
4 | g.95155662A>G | CA10622021 | BMPR1B | c.*989A>G (n.*989A>G) c.*13+976A>G (n.*13+976A>G) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.95155662A>C | CA1477970726 | BMPR1B | c.*989A>C (n.*989A>C) c.*13+976A>C (n.*13+976A>C) | dbSNP |