| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 17 | g.72124275A>G | CA16620598 | SOX9 | c.1418A>G (p.Gln473Arg) | ClinVar dbSNP COSMIC |
| 17 | g.72124275A>T | CA400868410 | SOX9 | c.1418A>T (p.Gln473Leu) | dbSNP |
| 17 | g.72124275A>C | CA400868409 | SOX9 | c.1418A>C (p.Gln473Pro) | dbSNP |