| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.176093573G>A | CA349353265 | HOXD13 | c.683G>A (p.Gly228Glu) c.725-907G>A (n.725-907G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.176093573G>C | CA16040613 | HOXD13 | c.683G>C (p.Gly228Ala) c.725-907G>C (n.725-907G>C) | ClinVar dbSNP |
| 2 | g.176093573G>T | CA124419 | HOXD13 | c.683G>T (p.Gly228Val) c.725-907G>T (n.725-907G>T) | ClinVar dbSNP |