Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.97305364C>TCA228097DPYD,DPYD-AS1c.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
1g.97305364C>GCA341375219DPYD,DPYD-AS1c.2194G>C (p.Val732Leu)
n.129-825C>G
c.1978G>C (p.Val660Leu)
c.2083G>C (p.Val695Leu)
c.1699G>C (p.Val567Leu)
dbSNP
1g.97305364C=CA1139894831DPYD,DPYD-AS1c.2194G= (p.Val732=)
n.129-825C=
c.1978G= (p.Val660=)
c.2083G= (p.Val695=)
c.1699G= (p.Val567=)
dbSNP dbSNP
1g.97305364C>ACA341375218DPYD,DPYD-AS1c.2194G>T (p.Val732Phe)
n.129-825C>A
c.1978G>T (p.Val660Phe)
c.2083G>T (p.Val695Phe)
c.1699G>T (p.Val567Phe)
dbSNP

Number of alleles fetched