"Fulgent Genetics, Fulgent Genetics"[submitter] AND "HPD"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 459972	NM_002150.3(HPD):c.813C>T (p.Thr271=)	HPD	Single nucleotide variant (synonymous variant)	Hawkinsinuria +1 more	GBenign/Likely benign
Select item 307485	NM_002150.3(HPD):c.414G>A (p.Thr138=)	HPD	Single nucleotide variant (synonymous variant)	Hawkinsinuria +2 more	GBenign/Likely benign
Select item 1042401	NM_002150.3(HPD):c.356G>A (p.Arg119Gln)	HPD (R80Q +1 more)	Single nucleotide variant (missense variant)	Tyrosinemia type III +2 more	GUncertain significance
Select item 1123241	NM_002150.3(HPD):c.325-19G>C	HPD	Single nucleotide variant (intron variant)	Hawkinsinuria +1 more	GLikely benign
Select item 802899	NM_002150.3(HPD):c.97A>G (p.Thr33Ala)	HPD (T33A)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +3 more	GBenign

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