| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.24990569G>C | CA2164998832 | SNHG14 | c.*953+8132G>C (n.*953+8132G>C) c.*400-8401G>C (n.*400-8401G>C) n.3625-7797G>C | dbSNP |
| 15 | g.24990569G>A | CA15836280 | SNHG14 | c.*953+8132G>A (n.*953+8132G>A) c.*400-8401G>A (n.*400-8401G>A) n.3625-7797G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |