Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.49667554T>A | CA1363594777 | BSN | c.*105-36T>A (n.*105-36T>A) | dbSNP gnomAD v4 |
3 | g.49667554T>G | CA1363594776 | BSN | c.*105-36T>G (n.*105-36T>G) | dbSNP |
3 | g.49667554T>C | CA15228614 | BSN | c.*105-36T>C (n.*105-36T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |