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Variants (4)
| CIViC ID | Name | HGVS | Type(s) |
|---|---|---|---|
| 738 | DPYD*13 HOMOZYGOSITY RS55886062,ILE560SER,I560S | NM_000110.3:c.1679T>G,NP_000101.2:p.Ile560Ser,ENST00000370192.3:c.1679T>G,NC_000001.10:g.97981343A>C | missense_variant |
| 737 | DPYD*2A HOMOZYGOSITY RS3918290,DPYD*2A,DPYD:IVS14 + 1G>A,C.1905+1G>A | NC_000001.10:g.97915614C>T,NM_000110.3:c.1905+1G>A,ENST00000370192.3:c.1905+1G>A | splice_donor_variant |
| 2893 | EXON 11-19 DELETION | inframe_deletion | |
| 740 | RS67376798 HOMOZYGOSITY C.2846A>T,P.ASP949VAL,N949V | polymorphic_sequence_variant |