| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.55223902C>G | CA117892 | RAB27A | n.2490G>C c.454G>C (p.Ala152Pro) n.2622G>C | ClinVar dbSNP |
| 15 | g.55223902C>T | CA392529511 | RAB27A | n.2490G>A c.454G>A (p.Ala152Thr) n.2622G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.55223902C= | CA2178720777 | RAB27A | n.2490G= c.454G= (p.Ala152=) n.2622G= | dbSNP |