Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.159315942T>A | CA1083506148 | IL12B | c.*159A>T (n.*159A>T) c.*641A>T (n.*641A>T) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.159315942T>G | CA10621150 | IL12B | c.*159A>C (n.*159A>C) c.*641A>C (n.*641A>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |