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

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3218313	NM_005040.4(PRCP):c.1443G>A (p.Met481Ile)	PRCP (M481I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350278	NM_005040.4(PRCP):c.1439A>G (p.His480Arg)	PRCP (H480R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218312	NM_005040.4(PRCP):c.1404G>A (p.Met468Ile)	PRCP (M363I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378430	NM_005040.4(PRCP):c.1379G>A (p.Arg460His)	PRCP (R355H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463574	NM_005040.4(PRCP):c.1378C>T (p.Arg460Cys)	PRCP (R460C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307733	NM_005040.4(PRCP):c.1342G>T (p.Val448Phe)	PRCP (V343F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570325	NM_005040.4(PRCP):c.1304G>A (p.Gly435Asp)	PRCP (G435D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218310	NM_005040.4(PRCP):c.1243A>G (p.Asn415Asp)	PRCP (N436D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236704	NM_005040.4(PRCP):c.1225A>G (p.Thr409Ala)	PRCP (T304A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487668	NM_005040.4(PRCP):c.1222A>C (p.Thr408Pro)	PRCP (T408P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588087	NM_005040.4(PRCP):c.1129G>A (p.Asp377Asn)	PRCP (D272N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356052	NM_005040.4(PRCP):c.991C>G (p.Leu331Val)	PRCP (L226V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401175	NM_005040.4(PRCP):c.855T>A (p.Asn285Lys)	PRCP (N285K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476031	NM_005040.4(PRCP):c.717G>T (p.Arg239Ser)	PRCP (R260S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455994	NM_005040.4(PRCP):c.688G>A (p.Gly230Ser)	PRCP (G230S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375837	NM_005040.4(PRCP):c.681G>C (p.Arg227Ser)	PRCP (R227S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543038	NM_005040.4(PRCP):c.626T>C (p.Phe209Ser)	PRCP (F209S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598376	NM_005040.4(PRCP):c.624G>C (p.Gln208His)	PRCP (Q103H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309730	NM_005040.4(PRCP):c.488G>A (p.Arg163Lys)	PRCP (R58K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309732	NM_005040.4(PRCP):c.348G>A (p.Met116Ile)	PRCP (M137I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455115	NM_005040.4(PRCP):c.318G>A (p.Met106Ile)	PRCP (M1I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309728	NM_005040.4(PRCP):c.317T>C (p.Met106Thr)	PRCP (M127T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218314	NM_005040.4(PRCP):c.212G>A (p.Arg71Gln)	PRCP (R92Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3309729	NM_005040.4(PRCP):c.193G>C (p.Val65Leu)	PRCP (V65L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472638	NM_005040.4(PRCP):c.191C>T (p.Thr64Ile)	PRCP (T85I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335303	NM_005040.4(PRCP):c.58A>G (p.Ile20Val)	LOC130006517, PRCP (I20V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275178	NM_005040.4(PRCP):c.46C>T (p.Pro16Ser)	LOC130006517, PRCP (P16S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279519	NM_005040.4(PRCP):c.16C>T (p.Leu6Phe)	PRCP (L6F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 28