Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.97515787A>C | CA228118 | DPYD | c.1679T>G (p.Ile560Ser) c.1524+33773T>G (n.1524+33773T>G) c.1568T>G (p.Ile523Ser) c.1184T>G (p.Ile395Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.97515787A>T | CA27638125 | DPYD | c.1679T>A (p.Ile560Asn) c.1524+33773T>A (n.1524+33773T>A) c.1568T>A (p.Ile523Asn) c.1184T>A (p.Ile395Asn) | dbSNP |