| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.43126651C>T | CA009200 | RET | c.2720C>T (p.Pro907Leu) n.2690C>T c.3116C>T (p.Pro1039Leu) c.*1710C>T (n.*1710C>T) c.*465C>T (n.*465C>T) c.2354C>T (p.Pro785Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.43126651C>A | CA009192 | RET | c.2720C>A (p.Pro907Gln) n.2690C>A c.3116C>A (p.Pro1039Gln) c.*1710C>A (n.*1710C>A) c.*465C>A (n.*465C>A) c.2354C>A (p.Pro785Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.43126651C>G | CA376558427 | RET | c.2720C>G (p.Pro907Arg) n.2690C>G c.3116C>G (p.Pro1039Arg) c.*1710C>G (n.*1710C>G) c.*465C>G (n.*465C>G) c.2354C>G (p.Pro785Arg) | ClinVar dbSNP |