| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.65944422G>A | CA2042776051 | HMGA2 | c.250-6961G>A (n.250-6961G>A) c.287-6961G>A (n.287-6961G>A) | dbSNP |
| 12 | g.65944422G>T | CA15730419 | HMGA2 | c.250-6961G>T (n.250-6961G>T) c.287-6961G>T (n.287-6961G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.65944422G= | CA2042776052 | HMGA2 | c.250-6961G= (n.250-6961G=) c.287-6961G= (n.287-6961G=) | dbSNP |