"Ambry Genetics"[submitter] AND "HERPUD1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2472072	NM_014685.4(HERPUD1):c.22G>A (p.Glu8Lys)	HERPUD1 (E8K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380760	NM_014685.4(HERPUD1):c.295G>A (p.Ala99Thr)	HERPUD1 (A99T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3105475	NM_014685.4(HERPUD1):c.316G>A (p.Glu106Lys)	HERPUD1 (E105K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105476	NM_014685.4(HERPUD1):c.477C>G (p.Phe159Leu)	HERPUD1, LOC130059057 (F159L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105477	NM_014685.4(HERPUD1):c.912C>A (p.His304Gln)	HERPUD1, LOC130059059 (T252K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3105479	NM_014685.4(HERPUD1):c.941C>T (p.Pro314Leu)	HERPUD1 (P314L +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2510790	NM_014685.4(HERPUD1):c.980T>G (p.Val327Gly)	HERPUD1 (V326G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar