| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.7132230G>A | CA124223 | INSR | c.2770C>T (p.Arg924Ter) c.2734C>T (p.Arg912Ter) c.2848C>T (p.Arg950Ter) c.2812C>T (p.Arg938Ter) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 19 | g.7132230G>C | CA9135455 | INSR | c.2770C>G (p.Arg924Gly) c.2734C>G (p.Arg912Gly) c.2848C>G (p.Arg950Gly) c.2812C>G (p.Arg938Gly) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 19 | g.7132230G= | CA2320771076 | INSR | c.2770C= (p.Arg924=) c.2734C= (p.Arg912=) c.2848C= (p.Arg950=) c.2812C= (p.Arg938=) | dbSNP |