Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.241851760C>A | CA1339828855 | PDCD1 | c.627+189G>T (n.627+189G>T) c.301+189G>T c.*190+189G>T (n.*190+189G>T) | dbSNP |
2 | g.241851760C>G | CA120243 | PDCD1 | c.627+189G>C (n.627+189G>C) c.301+189G>C c.*190+189G>C (n.*190+189G>C) | ClinVar dbSNP |
2 | g.241851760C>T | CA11105434 | PDCD1 | c.627+189G>A (n.627+189G>A) c.301+189G>A c.*190+189G>A (n.*190+189G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |