ARPP21[gene] and "single gene"[properties] - ClinVar

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Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3129821	NM_001385562.1(ARPP21):c.103G>T (p.Asp35Tyr)	ARPP21 (D35Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129830	NM_001385562.1(ARPP21):c.271C>G (p.His91Asp)	ARPP21 (H91D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2212126	NM_001385562.1(ARPP21):c.280C>A (p.Leu94Ile)	ARPP21 (L94I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2653651	NM_001385562.1(ARPP21):c.320G>A (p.Arg107Lys)	ARPP21 (R101K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2488296	NM_001385562.1(ARPP21):c.535G>A (p.Ala179Thr)	ARPP21 (A179T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273910	NM_001385562.1(ARPP21):c.616T>C (p.Phe206Leu)	ARPP21 (F204L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368615	NM_001385562.1(ARPP21):c.665A>G (p.Asn222Ser)	ARPP21 (N216S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262832	NM_001385562.1(ARPP21):c.671C>A (p.Thr224Asn)	ARPP21 (T218N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316053	NM_001385562.1(ARPP21):c.704G>C (p.Cys235Ser)	ARPP21 (C233S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3316070	NM_001385562.1(ARPP21):c.747G>A (p.Arg249=)	ARPP21	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 2513353	NM_001385562.1(ARPP21):c.807G>C (p.Met269Ile)	ARPP21 (M1I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2281271	NM_001385562.1(ARPP21):c.918C>G (p.Ser306Arg)	ARPP21 (S270R +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2405825	NM_001385562.1(ARPP21):c.938G>A (p.Arg313Lys)	ARPP21 (G243S +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3316073	NM_001385562.1(ARPP21):c.965A>G (p.Asn322Ser)	ARPP21 (N287S +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2653652	NM_001385562.1(ARPP21):c.990C>G (p.Leu330=)	ARPP21 (S260C)	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign
Select item 3129819	NM_001385562.1(ARPP21):c.1009G>C (p.Gly337Arg)	ARPP21 (G277R +12 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2326720	NM_001385562.1(ARPP21):c.1024T>A (p.Ser342Thr)	ARPP21 (S285T +12 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129820	NM_001385562.1(ARPP21):c.1028G>A (p.Gly343Glu)	ARPP21 (G286E +12 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2592309	NM_001385562.1(ARPP21):c.1250G>A (p.Gly417Asp)	ARPP21 (G153D +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406883	NM_001385562.1(ARPP21):c.1298C>T (p.Pro433Leu)	ARPP21 (P149L +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129822	NM_001385562.1(ARPP21):c.1318G>A (p.Ala440Thr)	ARPP21 (A338T +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234733	NM_001385562.1(ARPP21):c.1327C>G (p.Pro443Ala)	ARPP21 (P341A +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344659	NM_001385562.1(ARPP21):c.1350G>C (p.Glu450Asp)	ARPP21 (E186D +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129823	NM_001385562.1(ARPP21):c.1353T>A (p.Asn451Lys)	ARPP21 (N163K +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161701	NM_001385562.1(ARPP21):c.1355G>T (p.Gly452Val)	ARPP21 (G452V +12 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance
Select item 3316042	NM_001385562.1(ARPP21):c.1417A>G (p.Thr473Ala)	ARPP21 (T417A +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129825	NM_001385562.1(ARPP21):c.1442T>G (p.Leu481Arg)	ARPP21 (L193R +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466676	NM_001385562.1(ARPP21):c.1505C>T (p.Pro502Leu)	ARPP21 (P218L +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316063	NM_001385562.1(ARPP21):c.1570C>G (p.Gln524Glu)	ARPP21 (Q377E +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261218	NM_001385562.1(ARPP21):c.1627G>A (p.Gly543Ser)	ARPP21 (G259S +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2653653	NM_001385562.1(ARPP21):c.1698T>C (p.Ser566=)	ARPP21	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2653654	NM_001385562.1(ARPP21):c.1888G>A (p.Ala630Thr)	ARPP21 (A342T +15 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3129826	NM_001385562.1(ARPP21):c.1895C>T (p.Thr632Ile)	ARPP21 (T368I +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316104	NM_001385562.1(ARPP21):c.1942A>G (p.Ile648Val)	ARPP21 (I613V +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129827	NM_001385562.1(ARPP21):c.2014C>G (p.Pro672Ala)	ARPP21 (P618A +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316082	NM_001385562.1(ARPP21):c.2071C>G (p.Pro691Ala)	ARPP21 (P638A +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384795	NM_001385562.1(ARPP21):c.2104A>T (p.Ser702Cys)	ARPP21 (S600C +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598386	NM_001385562.1(ARPP21):c.2123C>G (p.Ala708Gly)	ARPP21 (A561G +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243697	NM_001385562.1(ARPP21):c.2264A>G (p.Tyr755Cys)	ARPP21 (Y699C +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306573	NM_001385562.1(ARPP21):c.2269A>G (p.Thr757Ala)	ARPP21 (T473A +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2506387	NM_001385562.1(ARPP21):c.2325G>T (p.Gln775His)	ARPP21 (Q487H +15 more)	Single nucleotide variant (missense variant +1 more)	Monomelic amyotrophy	GUncertain significance
Select item 2261653	NM_001385562.1(ARPP21):c.2391G>A (p.Met797Ile)	ARPP21 (M533I +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316031	NM_001385562.1(ARPP21):c.2406T>A (p.Asn802Lys)	ARPP21 (N767K +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129829	NM_001385562.1(ARPP21):c.2447G>A (p.Gly816Asp)	ARPP21 (G532D +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316093	NM_001385562.1(ARPP21):c.2495G>A (p.Arg832Lys)	ARPP21 (R778K +12 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401563	NM_001385562.1(ARPP21):c.2517C>A (p.Ser839Arg)	ARPP21 (S782R +15 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 689176	GRCh37/hg19 3p22.3(chr3:35796715-35948815)x3	ARPP21	Copy number gain	not provided	GUncertain significance
Select item 687725	GRCh37/hg19 3p22.3(chr3:35796715-35948815)x3	ARPP21	Copy number gain	not provided	GUncertain significance
Select item 686431	GRCh37/hg19 3p22.3(chr3:35803643-35948815)x3	ARPP21	Copy number gain	not provided	GUncertain significance
Select item 221798	GRCh37/hg19 3p22.3(chr3:35832877-35925872)x3	ARPP21	Copy number gain	Premature ovarian failure	GBenign

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Items: 50