| 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 |
| 10 | g.43102596C>G | CA376543602 | RET | c.592C>G (p.Pro198Ala) c.513C>G c.494C>G c.534C>G c.365C>G c.74-8611C>G (n.74-8611C>G) c.74-9503C>G (n.74-9503C>G) | ClinVar dbSNP |
| 10 | g.43102596C= | CA1905805567 | RET | c.592C= (p.Pro198=) c.513C= c.494C= c.534C= c.365C= c.74-8611C= (n.74-8611C=) c.74-9503C= (n.74-9503C=) | dbSNP |