| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.149379110C>T | CA16042638 | TAB2 | n.1610C>T c.1195C>T (p.Gln399Ter) c.343C>T (p.Gln115Ter) c.1099C>T (p.Gln367Ter) | ClinVar dbSNP |
| 6 | g.149379110C= | CA1671916027 | TAB2 | n.1610C= c.1195C= (p.Gln399=) c.343C= (p.Gln115=) c.1099C= (p.Gln367=) | dbSNP |