| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.43102596C>T | CA376543603 | RET | c.592C>T (p.Pro198Ser) c.513C>T c.494C>T c.534C>T c.365C>T c.74-8611C>T (n.74-8611C>T) c.74-9503C>T (n.74-9503C>T) | ClinVar dbSNP gnomAD v4 |
| 10 | g.43102596C>A | CA009290 | RET | c.592C>A (p.Pro198Thr) c.513C>A c.494C>A c.534C>A c.365C>A c.74-8611C>A (n.74-8611C>A) c.74-9503C>A (n.74-9503C>A) | ClinVar dbSNP |