| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.203960563T>C | CA10613681 | ICOS | c.*964T>C (n.*964T>C) c.*972T>C (n.*972T>C) c.*1065T>C (n.*1065T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 2 | g.203960563T= | CA1322192323 | ICOS | c.*964T= (n.*964T=) c.*972T= (n.*972T=) c.*1065T= (n.*1065T=) | dbSNP |