| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.7125437C>A | CA124211 | INSR | c.3104G>T (p.Gly1035Val) c.3068G>T (p.Gly1023Val) c.3179G>T (p.Gly1060Val) c.3143G>T (p.Gly1048Val) c.3101G>T (p.Gly1034Val) c.3065G>T (p.Gly1022Val) | ClinVar dbSNP |
| 19 | g.7125437C= | CA2320767964 | INSR | c.3104G= (p.Gly1035=) c.3068G= (p.Gly1023=) c.3179G= (p.Gly1060=) c.3143G= (p.Gly1048=) c.3101G= (p.Gly1034=) c.3065G= (p.Gly1022=) | dbSNP |