Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.87683553T>A | CA1926059521 | PAPSS2 | c.27+23545T>A (n.27+23545T>A) n.49+23148T>A n.70+22500T>A | dbSNP |
10 | g.87683553T>C | CA13226306 | PAPSS2 | c.27+23545T>C (n.27+23545T>C) n.49+23148T>C n.70+22500T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |