| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.96193303T>C | CA13820377 | HS6ST3 | c.707+101734T>C (n.707+101734T>C) c.708-49353T>C (n.708-49353T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.96193303T= | CA2112648429 | HS6ST3 | c.707+101734T= (n.707+101734T=) c.708-49353T= (n.708-49353T=) | dbSNP |