Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.241851697G>A | CA11143161 | PDCD1 | c.627+252C>T (n.627+252C>T) c.301+252C>T c.*190+252C>T (n.*190+252C>T) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.241851697G>C | CA1339828808 | PDCD1 | c.627+252C>G (n.627+252C>G) c.301+252C>G c.*190+252C>G (n.*190+252C>G) | dbSNP |