"Ambry Genetics"[submitter] AND "PRH2"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3218642	NM_001110213.1(PRH2):c.98C>T (p.Ser33Leu)	PRH1, PRH1-PRR4 +1 more (S33L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309906	NM_001110213.1(PRH2):c.154G>C (p.Gly52Arg)	PRH1, PRH1-PRR4 +1 more (G52R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467372	NM_001110213.1(PRH2):c.193C>A (p.Gln65Lys)	PRH1, PRH1-PRR4 +1 more (Q65K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218636	NM_001110213.1(PRH2):c.212A>G (p.Gln71Arg)	PRH1, PRH1-PRR4 +1 more (Q71R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309905	NM_001110213.1(PRH2):c.220C>A (p.Pro74Thr)	PRH1, PRH1-PRR4 +1 more (P74T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322403	NM_001110213.1(PRH2):c.248G>A (p.Gly83Asp)	PRH1, PRH1-PRR4 +1 more (G83D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263155	NM_001110213.1(PRH2):c.265G>A (p.Gly89Arg)	PRH1, PRH1-PRR4 +1 more (G89R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218638	NM_001110213.1(PRH2):c.275A>G (p.Gln92Arg)	PRH1, PRH1-PRR4 +1 more (Q92R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353613	NM_001110213.1(PRH2):c.295G>T (p.Gly99Cys)	PRH1, PRH1-PRR4 +1 more (G99C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218639	NM_001110213.1(PRH2):c.298C>A (p.His100Asn)	PRH1, PRH1-PRR4 +1 more (H100N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218640	NM_001110213.1(PRH2):c.301C>A (p.Pro101Thr)	PRH1, PRH1-PRR4 +1 more (P101T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254330	NM_001110213.1(PRH2):c.356G>C (p.Arg119Pro)	PRH1, PRH1-PRR4 +1 more (R119P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405564	NM_001110213.1(PRH2):c.365G>A (p.Arg122Gln)	PRH1, PRH1-PRR4 +1 more (R122Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610319	NM_001110213.1(PRH2):c.422C>T (p.Pro141Leu)	PRH1, PRH1-PRR4 +1 more (P141L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218641	NM_001110213.1(PRH2):c.482A>T (p.Gln161Leu)	PRH1, PRH1-PRR4 +1 more (Q161L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance