"Ambry Genetics"[submitter] AND "PRRG2"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2462937	NM_000951.3(PRRG2):c.97G>A (p.Gly33Ser)	PRRG2 (G10S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467073	NM_000951.3(PRRG2):c.100C>T (p.Pro34Ser)	PRRG2 (P11S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2507722	NM_000951.3(PRRG2):c.101C>G (p.Pro34Arg)	PRRG2 (P34R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219721	NM_000951.3(PRRG2):c.149C>A (p.Ala50Asp)	PRRG2 (A50D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230311	NM_000951.3(PRRG2):c.164T>C (p.Leu55Pro)	PRRG2 (L32P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276813	NM_000951.3(PRRG2):c.229G>A (p.Ala77Thr)	PRRG2 (A54T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310588	NM_000951.3(PRRG2):c.259A>G (p.Thr87Ala)	PRRG2 (T64A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219723	NM_000951.3(PRRG2):c.266G>A (p.Arg89His)	PRRG2 (R66H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375175	NM_000951.3(PRRG2):c.325A>T (p.Ser109Cys)	PRRG2 (S86C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310587	NM_000951.3(PRRG2):c.350G>T (p.Gly117Val)	PRRG2 (G117V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219724	NM_000951.3(PRRG2):c.373G>T (p.Gly125Cys)	PRRG2 (G102C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339371	NM_000951.3(PRRG2):c.373G>A (p.Gly125Ser)	PRRG2 (G125S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320403	NM_000951.3(PRRG2):c.398G>A (p.Arg133His)	PRRG2 (R110H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2368898	NM_000951.3(PRRG2):c.404G>A (p.Arg135Gln)	PRRG2 (R112Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341674	NM_000951.3(PRRG2):c.475C>G (p.Leu159Val)	PRRG2 (L136V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310323	NM_000951.3(PRRG2):c.478G>C (p.Gly160Arg)	PRRG2 (G137R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310590	NM_000951.3(PRRG2):c.491C>G (p.Pro164Arg)	PRRG2 (P164R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3219725	NM_000951.3(PRRG2):c.502C>A (p.Pro168Thr)	PRRG2 (P168T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310589	NM_000951.3(PRRG2):c.577C>T (p.Pro193Ser)	LOC130064928, PRRG2 (P170S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513092	NM_000951.3(PRRG2):c.580C>T (p.Pro194Ser)	LOC130064928, PRRG2 (P171S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353254	NM_000951.3(PRRG2):c.580C>G (p.Pro194Ala)	LOC130064928, PRRG2 (P171A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310586	NM_000951.3(PRRG2):c.581C>T (p.Pro194Leu)	LOC130064928, PRRG2 (P194L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 22