| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89935700G>C | CA340622 | TUBB3 | c.1249G>C (p.Asp417His) n.4670G>C c.1033G>C (p.Asp345His) c.277+2122G>C (n.277+2122G>C) c.*1334G>C (n.*1334G>C) c.2290G>C (p.Asp764His) | ClinVar dbSNP |
| 16 | g.89935700G>A | CA340624 | TUBB3 | c.1249G>A (p.Asp417Asn) n.4670G>A c.1033G>A (p.Asp345Asn) c.277+2122G>A (n.277+2122G>A) c.*1334G>A (n.*1334G>A) c.2290G>A (p.Asp764Asn) | ClinVar dbSNP COSMIC |