PIWIL3[gene] and "single gene"[properties] - ClinVar

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Items: 65

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 782793	NM_001255975.1(PIWIL3):c.2605C>T (p.Arg869Cys)	PIWIL3 (R878C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2368193	NM_001255975.1(PIWIL3):c.2575C>A (p.His859Asn)	PIWIL3 (H859N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329785	NM_001255975.1(PIWIL3):c.2521C>G (p.Pro841Ala)	PIWIL3 (P841A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213366	NM_001255975.1(PIWIL3):c.2471C>T (p.Thr824Ile)	PIWIL3 (T824I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2217625	NM_001255975.1(PIWIL3):c.2465G>A (p.Arg822His)	PIWIL3 (R822H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252165	NM_001255975.1(PIWIL3):c.2464C>T (p.Arg822Cys)	PIWIL3 (R822C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307187	NM_001255975.1(PIWIL3):c.2440G>A (p.Gly814Ser)	PIWIL3 (G814S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246654	NM_001255975.1(PIWIL3):c.2422G>A (p.Val808Ile)	PIWIL3 (V808I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406138	NM_001255975.1(PIWIL3):c.2370T>G (p.Phe790Leu)	PIWIL3 (F799L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455462	NM_001255975.1(PIWIL3):c.2294G>A (p.Gly765Glu)	PIWIL3 (G774E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213364	NM_001255975.1(PIWIL3):c.2273C>T (p.Thr758Ile)	PIWIL3 (T758I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559410	NM_001255975.1(PIWIL3):c.2243C>A (p.Ala748Asp)	PIWIL3 (A748D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335751	NM_001255975.1(PIWIL3):c.2199G>A (p.Met733Ile)	PIWIL3 (M733I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343644	NM_001255975.1(PIWIL3):c.2114C>T (p.Ser705Leu)	PIWIL3 (S705L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2279069	NM_001255975.1(PIWIL3):c.2013G>C (p.Trp671Cys)	PIWIL3 (W680C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477906	NM_001255975.1(PIWIL3):c.1991C>T (p.Thr664Ile)	PIWIL3 (T664I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2530524	NM_001255975.1(PIWIL3):c.1890G>C (p.Trp630Cys)	PIWIL3 (W639C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486143	NM_001255975.1(PIWIL3):c.1762T>C (p.Tyr588His)	PIWIL3 (Y588H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401530	NM_001255975.1(PIWIL3):c.1742G>A (p.Arg581Lys)	PIWIL3 (R581K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221628	NM_001255975.1(PIWIL3):c.1739G>A (p.Arg580His)	PIWIL3 (R580H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3213362	NM_001255975.1(PIWIL3):c.1734C>A (p.Asp578Glu)	PIWIL3 (D587E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213361	NM_001255975.1(PIWIL3):c.1691G>T (p.Arg564Ile)	PIWIL3 (R564I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213360	NM_001255975.1(PIWIL3):c.1681A>G (p.Lys561Glu)	PIWIL3 (K561E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516675	NM_001255975.1(PIWIL3):c.1678C>T (p.Arg560Trp)	PIWIL3 (R560W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555692	NM_001255975.1(PIWIL3):c.1666A>G (p.Ile556Val)	PIWIL3 (I556V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213359	NM_001255975.1(PIWIL3):c.1523A>G (p.His508Arg)	PIWIL3 (H508R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3306770	NM_001255975.1(PIWIL3):c.1448T>C (p.Met483Thr)	PIWIL3 (M483T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213358	NM_001255975.1(PIWIL3):c.1437A>C (p.Gln479His)	PIWIL3 (Q479H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220083	NM_001255975.1(PIWIL3):c.1426A>C (p.Asn476His)	PIWIL3 (N476H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387815	NM_001255975.1(PIWIL3):c.1399G>A (p.Val467Ile)	PIWIL3 (V467I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335300	NM_001255975.1(PIWIL3):c.1395G>T (p.Leu465Phe)	PIWIL3 (L465F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306382	NM_001255975.1(PIWIL3):c.1381G>C (p.Asp461His)	PIWIL3 (D461H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534078	NM_001255975.1(PIWIL3):c.1297C>A (p.His433Asn)	PIWIL3 (H433N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556968	NM_001255975.1(PIWIL3):c.1212G>A (p.Met404Ile)	PIWIL3 (M404I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2228419	NM_001255975.1(PIWIL3):c.1195C>A (p.Pro399Thr)	PIWIL3 (P399T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600390	NM_001255975.1(PIWIL3):c.1094A>G (p.His365Arg)	PIWIL3 (H365R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 711766	NM_001255975.1(PIWIL3):c.970C>G (p.Leu324Val)	PIWIL3 (L324V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3306771	NM_001255975.1(PIWIL3):c.871A>G (p.Ile291Val)	PIWIL3 (I291V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407749	NM_001255975.1(PIWIL3):c.811G>A (p.Val271Ile)	PIWIL3 (V271I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2547373	NM_001255975.1(PIWIL3):c.748A>G (p.Lys250Glu)	PIWIL3 (K250E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213370	NM_001255975.1(PIWIL3):c.736T>A (p.Tyr246Asn)	PIWIL3 (Y246N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213369	NM_001255975.1(PIWIL3):c.650C>A (p.Thr217Lys)	PIWIL3 (T217K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213607	NM_001255975.1(PIWIL3):c.586A>G (p.Ser196Gly)	PIWIL3 (S196G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 777674	NM_001255975.1(PIWIL3):c.557C>T (p.Pro186Leu)	PIWIL3 (P186L)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 781524	NM_001255975.1(PIWIL3):c.551C>T (p.Ser184Phe)	PIWIL3 (S184F)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 711780	NM_001255975.1(PIWIL3):c.517C>T (p.Arg173Cys)	PIWIL3 (R173C)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3306769	NM_001255975.1(PIWIL3):c.475C>T (p.Arg159Cys)	PIWIL3 (R159C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306432	NM_001255975.1(PIWIL3):c.472C>A (p.Leu158Ile)	PIWIL3 (L158I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3306773	NM_001255975.1(PIWIL3):c.458T>C (p.Ile153Thr)	PIWIL3 (I153T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3306772	NM_001255975.1(PIWIL3):c.421G>T (p.Val141Phe)	PIWIL3 (V141F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386542	NM_001255975.1(PIWIL3):c.409C>T (p.Arg137Cys)	PIWIL3 (R137C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 711781	NM_001255975.1(PIWIL3):c.376C>G (p.Gln126Glu)	PIWIL3 (Q126E)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3213368	NM_001255975.1(PIWIL3):c.370G>A (p.Val124Met)	PIWIL3 (V124M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556882	NM_001255975.1(PIWIL3):c.338T>C (p.Val113Ala)	PIWIL3 (V113A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284600	NM_001255975.1(PIWIL3):c.324A>T (p.Gln108His)	PIWIL3 (Q108H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284598	NM_001255975.1(PIWIL3):c.323A>T (p.Gln108Leu)	PIWIL3 (Q108L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 769159	NM_001255975.1(PIWIL3):c.267C>T (p.Pro89=)	PIWIL3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2221977	NM_001255975.1(PIWIL3):c.265C>G (p.Pro89Ala)	PIWIL3 (P89A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2268761	NM_001255975.1(PIWIL3):c.257A>C (p.His86Pro)	PIWIL3 (H86P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248082	NM_001255975.1(PIWIL3):c.235C>T (p.Pro79Ser)	PIWIL3 (P79S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2523248	NM_001255975.1(PIWIL3):c.173T>C (p.Leu58Pro)	PIWIL3 (L58P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466936	NM_001255975.1(PIWIL3):c.136C>T (p.Arg46Trp)	PIWIL3 (R46W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589580	NM_001255975.1(PIWIL3):c.134C>T (p.Pro45Leu)	PIWIL3 (P45L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554807	NM_001255975.1(PIWIL3):c.119A>G (p.Gln40Arg)	PIWIL3 (Q40R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358727	NM_001255975.1(PIWIL3):c.76G>A (p.Gly26Arg)	PIWIL3 (G26R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 65