ClinVar for Gene (Select 23548) - ClinVar

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Links from Gene

Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329878	NM_012382.3(TTC33):c.476T>C (p.Met159Thr)	PTGER4, TTC33 (M159T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184306	NM_012382.3(TTC33):c.611A>G (p.Tyr204Cys)	PTGER4, TTC33 (Y204C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184305	NM_012382.3(TTC33):c.505T>C (p.Ser169Pro)	PTGER4, TTC33 (S169P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184304	NM_012382.3(TTC33):c.136C>T (p.Arg46Cys)	TTC33 (R46C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2611255	NM_012382.3(TTC33):c.557A>G (p.Lys186Arg)	PTGER4, TTC33 (K186R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591781	NM_012382.3(TTC33):c.227G>A (p.Arg76Gln)	PTGER4, TTC33 (R76Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542475	NM_012382.3(TTC33):c.428T>G (p.Ile143Arg)	PTGER4, TTC33 (I143R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515490	NM_012382.3(TTC33):c.226C>T (p.Arg76Trp)	PTGER4, TTC33 (R76W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483905	NM_012382.3(TTC33):c.13G>A (p.Gly5Arg)	TTC33 (G5R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461476	NM_012382.3(TTC33):c.743A>G (p.Asp248Gly)	PTGER4, TTC33 (D248G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397536	NM_012382.3(TTC33):c.581C>T (p.Thr194Ile)	PTGER4, TTC33 (T194I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382289	NM_012382.3(TTC33):c.377C>T (p.Ser126Leu)	PTGER4, TTC33 (S126L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298273	NM_012382.3(TTC33):c.130A>G (p.Ile44Val)	TTC33 (I44V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271869	NM_012382.3(TTC33):c.56C>G (p.Ser19Cys)	TTC33 (S19C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225599	NM_012382.3(TTC33):c.403C>T (p.Arg135Cys)	PTGER4, TTC33 (R135C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204673	NM_012382.3(TTC33):c.518C>T (p.Thr173Met)	PTGER4, TTC33 (T173M)	Single nucleotide variant (missense variant)	not specified	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 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 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 560053	Single allele	C9, DAB2 +24 more	Deletion	not provided	GUncertain significance
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
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 148227	GRCh38/hg38 5p13.2-q12.1(chr5:35201559-61903141)x3	LINC02057, LINC02101 +518 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 58093	GRCh38/hg38 5p13.2-q11.1(chr5:36374107-51103841)x3	ANXA2R, ANXA2R-AS1 +245 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 58067	GRCh38/hg38 5p15.33-12(chr5:54839-45649861)x3	ADAMTS12, ADAMTS16 +952 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 38