Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97305364C>T | CA228097 | DPYD,DPYD-AS1 | c.2194G>A (p.Val732Ile) n.129-825C>T c.1978G>A (p.Val660Ile) c.2083G>A (p.Val695Ile) c.1699G>A (p.Val567Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.97305364C>G | CA341375219 | DPYD,DPYD-AS1 | c.2194G>C (p.Val732Leu) n.129-825C>G c.1978G>C (p.Val660Leu) c.2083G>C (p.Val695Leu) c.1699G>C (p.Val567Leu) | dbSNP |