"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "DPYD"[g - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 100069	NM_000110.4(DPYD):c.3067C>A (p.Pro1023Thr)	DPYD (P1023T)	Single nucleotide variant (missense variant)	Dihydropyrimidine dehydrogenase deficiency +2 more	GConflicting classifications of pathogenicity
Select item 715550	NM_000110.4(DPYD):c.2915A>G (p.Gln972Arg)	DPYD (Q972R)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 764540	NM_000110.4(DPYD):c.2623-8C>T	DPYD, DPYD-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 774156	NM_000110.4(DPYD):c.2299+7G>A	DPYD, DPYD-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 874135	NM_000110.4(DPYD):c.2279C>T (p.Thr760Ile)	DPYD, DPYD-AS1 (T760I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 735872	NM_000110.4(DPYD):c.2180-3T>C	DPYD, DPYD-AS1	Single nucleotide variant (intron variant)	Dihydropyrimidine dehydrogenase deficiency +2 more	GBenign/Likely benign
Select item 100087	NM_000110.4(DPYD):c.1905C>T (p.Asn635=)	DPYD	Single nucleotide variant (synonymous variant)	Dihydropyrimidine dehydrogenase deficiency +2 more	GConflicting classifications of pathogenicity
Select item 738289	NM_000110.4(DPYD):c.1701A>T (p.Gly567=)	DPYD	Single nucleotide variant (synonymous variant)	Dihydropyrimidine dehydrogenase deficiency +2 more	GLikely benign
Select item 711962	NM_000110.4(DPYD):c.1494A>G (p.Gln498=)	DPYD	Single nucleotide variant (synonymous variant)	Dihydropyrimidine dehydrogenase deficiency +2 more	GBenign/Likely benign
Select item 100097	NM_000110.4(DPYD):c.1371C>T (p.Asn457=)	DPYD	Single nucleotide variant (synonymous variant)	Dihydropyrimidine dehydrogenase deficiency +2 more	GBenign/Likely benign
Select item 100101	NM_000110.4(DPYD):c.1218G>A (p.Met406Ile)	DPYD (M406I)	Single nucleotide variant (missense variant)	Dihydropyrimidine dehydrogenase deficiency +2 more	GConflicting classifications of pathogenicity
Select item 585804	NM_000110.4(DPYD):c.681-8C>T	DPYD	Single nucleotide variant (intron variant)	Dihydropyrimidine dehydrogenase deficiency +1 more	GBenign/Likely benign
Select item 633188	NM_000110.4(DPYD):c.451A>G (p.Asn151Asp)	DPYD (N151D)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 788079	NM_000110.4(DPYD):c.258G>A (p.Pro86=)	DPYD	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 435	NM_000110.4(DPYD):c.85T>C (p.Cys29Arg)	DPYD (C29R)	Single nucleotide variant (missense variant)	capecitabine response - Toxicity +1 more	Gdrug response