PAIP1[gene] - ClinVar

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Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 149824	GRCh38/hg38 5p15.33-q13.3(chr5:22149-74412725)x3	ACTBL2, ADAMTS12 +1445 more	Copy number gain	See cases	GPathogenic
Select item 146130	GRCh38/hg38 5p15.33-11(chr5:49978-46114984)x3	ADAMTS12, ADAMTS16 +953 more	Copy number gain	See cases	GPathogenic
Select item 58067	GRCh38/hg38 5p15.33-12(chr5:54839-45649861)x3	ADAMTS12, ADAMTS16 +952 more	Copy number gain	See cases	GPathogenic
Select item 2683745	GRCh38/hg38 5p13.3-12(chr5:29299893-45899898)x3	AGXT2, LOC121725200 +385 more	Copy number gain	See cases	GLikely pathogenic
Select item 148227	GRCh38/hg38 5p13.2-q12.1(chr5:35201559-61903141)x3	LOC126807363, LOC126807364 +518 more	Copy number gain	See cases	GPathogenic
Select item 58092	GRCh38/hg38 5p13.2-12(chr5:35700480-45260029)x3	LOC126807367, LOC126807368 +254 more	Copy number gain	See cases	GPathogenic
Select item 58093	GRCh38/hg38 5p13.2-q11.1(chr5:36374107-51103841)x3	ANXA2R, ANXA2R-AS1 +245 more	Copy number gain	See cases	GPathogenic
Select item 2496000	NM_006451.5(PAIP1):c.1336G>C (p.Ala446Pro)	PAIP1 (A367P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259751	NM_006451.5(PAIP1):c.1145C>T (p.Ala382Val)	PAIP1 (A270V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357856	NM_006451.5(PAIP1):c.1054G>A (p.Val352Ile)	PAIP1 (V240I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553039	NM_006451.5(PAIP1):c.1021G>C (p.Asp341His)	PAIP1 (D262H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271453	NM_006451.5(PAIP1):c.910C>G (p.Leu304Val)	PAIP1 (L304V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208026	NM_006451.5(PAIP1):c.797G>T (p.Arg266Leu)	PAIP1 (R154L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523853	NM_006451.5(PAIP1):c.740G>A (p.Arg247Gln)	PAIP1 (R135Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320754	NM_006451.5(PAIP1):c.716G>T (p.Arg239Leu)	PAIP1 (R239L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393709	NM_006451.5(PAIP1):c.415G>A (p.Gly139Ser)	PAIP1 (G60S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323811	NM_006451.5(PAIP1):c.380A>G (p.Lys127Arg)	PAIP1 (K48R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405797	NM_006451.5(PAIP1):c.290C>T (p.Pro97Leu)	PAIP1 (P97L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250104	NM_006451.5(PAIP1):c.197C>G (p.Pro66Arg)	LOC129993869, PAIP1 (P66R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534380	NM_006451.5(PAIP1):c.193A>G (p.Thr65Ala)	LOC129993869, PAIP1 (T65A)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3208025	NM_006451.5(PAIP1):c.140A>G (p.Gln47Arg)	LOC129993869, PAIP1 (Q47R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262259	NM_006451.5(PAIP1):c.137C>T (p.Pro46Leu)	LOC129993869, PAIP1 (P46L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487305	NM_006451.5(PAIP1):c.134C>T (p.Pro45Leu)	LOC129993869, PAIP1 (P45L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353823	NM_006451.5(PAIP1):c.127C>T (p.His43Tyr)	LOC129993869, PAIP1 (H43Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517774	NM_006451.5(PAIP1):c.121G>C (p.Ala41Pro)	LOC129993869, PAIP1 (A41P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2287863	NM_006451.5(PAIP1):c.88G>A (p.Gly30Ser)	LOC129993869, PAIP1 (G30S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411830	NM_006451.5(PAIP1):c.58G>A (p.Gly20Ser)	LOC129993869, PAIP1 (G20S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3246316	NC_000005.9:g.(?_42688972)_(45303961_?)dup	ANXA2R, C5orf34 +12 more	Duplication	Early infantile epileptic encephalopathy with suppression bursts	GUncertain significance
Select item 1808669	GRCh37/hg19 5p13.3-11(chr5:29348753-46389339)x3	ADAMTS12, AGXT2 +71 more	Copy number gain	not provided	GPathogenic
Select item 1705919	GRCh37/hg19 5p13.2-11(chr5:36053583-46389339)x3	ANXA2R, C5orf34 +45 more	Copy number gain	musculoskeletal system issues	GPathogenic
Select item 1527153	GRCh37/hg19 5p14.1-11(chr5:26382110-46389339)	ADAMTS12, AGXT2 +72 more	Copy number gain	not specified	GPathogenic
Select item 1458418	NC_000005.9:g.(?_42688972)_(44388784_?)del	C5orf34, CCL28 +10 more	Deletion	not provided	GPathogenic
Select item 1180548	GRCh37/hg19 5p13.2-11(chr5:34984696-46405042)x3	AGXT2, ANXA2R +51 more	Copy number gain	not provided	GPathogenic
Select item 1012370	GRCh37/hg19 5p13.3-12(chr5:29081195-45294031)x3	ADAMTS12, AGXT2 +71 more	Copy number gain	See cases	GPathogenic
Select item 814684	GRCh37/hg19 5p13.1-q11.1(chr5:38432180-49441945)x3	GHR, CARD6 +31 more	Copy number gain	not provided	GPathogenic
Select item 687304	GRCh37/hg19 5p13.2-11(chr5:34453883-46389339)x3	AGXT2, ANXA2R +56 more	Copy number gain	not provided	GPathogenic
Select item 687006	GRCh37/hg19 5p12(chr5:43383397-43687730)x3	C5orf34, CCL28 +3 more	Copy number gain	not provided	GUncertain significance
Select item 635930	Single allele	C5orf24, C5orf34 +600 more	Deletion	Neurodevelopmental disorder	GUncertain significance
Select item 563053	GRCh37/hg19 5p14.1-12(chr5:27227243-45685844)x3	C1QTNF3, C5orf22 +71 more	Copy number gain	not provided	GPathogenic
Select item 442809	GRCh37/hg19 5p14.2-11(chr5:24281195-46389339)x3	ADAMTS12, AGXT2 +73 more	Copy number gain	See cases	GLikely pathogenic
Select item 442431	GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1	DHFR, DHX29 +738 more	Copy number loss	See cases	GPathogenic
Select item 441920	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 441919	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 253597	GRCh37/hg19 5p15.2-12(chr5:13461664-46098927)x3	RXFP3, GDNF +89 more	Copy number gain	See cases	GPathogenic

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Items: 44