Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.96365294G>C | CA2112592863 | HS6ST3 | c.707+273725G>C (n.707+273725G>C) c.708-267781G>C (n.708-267781G>C) c.708-122921G>C (n.708-122921G>C) | dbSNP |
13 | g.96365294G>A | CA13820396 | HS6ST3 | c.707+273725G>A (n.707+273725G>A) c.708-267781G>A (n.708-267781G>A) c.708-122921G>A (n.708-122921G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |