| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.7184511A>C | CA403670124 | INSR | c.779T>G (p.Leu260Arg) n.754T>G c.857T>G (p.Leu286Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 19 | g.7184511A>G | CA124227 | INSR | c.779T>C (p.Leu260Pro) n.754T>C c.857T>C (p.Leu286Pro) | ClinVar dbSNP |
| 19 | g.7184511A= | CA2320796303 | INSR | c.779T= (p.Leu260=) n.754T= c.857T= (p.Leu286=) | dbSNP |