ClinVar for Gene (Select 100128927) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3192089	NM_001137601.3(ZBTB42):c.80C>T (p.Thr27Ile)	ZBTB42 (T27I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192087	NM_001137601.3(ZBTB42):c.737C>T (p.Pro246Leu)	ZBTB42 (P246L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3192086	NM_001137601.3(ZBTB42):c.599G>A (p.Arg200Gln)	ZBTB42 (R200Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192085	NM_001137601.3(ZBTB42):c.181C>A (p.Arg61Ser)	ZBTB42 (R61S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192084	NM_001137601.3(ZBTB42):c.156C>G (p.Phe52Leu)	ZBTB42 (F52L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192083	NM_001137601.3(ZBTB42):c.1249G>A (p.Val417Ile)	ZBTB42 (V417I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192082	NM_001137601.3(ZBTB42):c.1061G>A (p.Arg354Gln)	ZBTB42 (R354Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063327	GRCh37/hg19 14q32.31-32.33(chr14:102098959-107285437)x1	ADSS1, AHNAK2 +65 more	Copy number loss	not specified	GPathogenic
Select item 3047052	NM_001137601.3(ZBTB42):c.333C>A (p.Val111=)	ZBTB42	Single nucleotide variant (synonymous variant)	ZBTB42-related condition	GLikely benign
Select item 3046269	NM_001137601.3(ZBTB42):c.879C>A (p.Leu293=)	ZBTB42	Single nucleotide variant (synonymous variant)	ZBTB42-related condition	GLikely benign
Select item 2685500	GRCh37/hg19 14q32.2-32.33(chr14:101024609-107285437)x1	DIO3OS, WDR20 +91 more	Copy number loss	not provided	GPathogenic
Select item 2684747	GRCh37/hg19 14q32.33(chr14:105122914-107285437)x3	ADSS1, AHNAK2 +32 more	Copy number gain	not provided	GUncertain significance
Select item 2684743	GRCh37/hg19 14q31.3-32.33(chr14:88580184-107285437)x3	ADSS1, AHNAK2 +182 more	Copy number gain	not provided	GPathogenic
Select item 2684728	GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3	ACOT4, ACOT6 +353 more	Copy number gain	not provided	GPathogenic
Select item 2579167	GRCh38/hg38 14q32.31-32.33(chr14:102263440-106874929)x1	MIR4538, MIR4539 +397 more	Copy number loss	Neurodevelopmental disorder	GPathogenic
Select item 2577008	GRCh37/hg19 14q32.32-32.33(chr14:103636647-107285437)x1	ADSS1, AHNAK2 +50 more	Copy number loss	not provided	GPathogenic
Select item 2547987	NM_001137601.3(ZBTB42):c.707G>A (p.Ser236Asn)	ZBTB42 (S236N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534760	NM_001137601.3(ZBTB42):c.187A>C (p.Thr63Pro)	ZBTB42 (T63P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534758	NM_001137601.3(ZBTB42):c.165C>G (p.Asp55Glu)	ZBTB42 (D55E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529447	NM_001137601.3(ZBTB42):c.1178G>A (p.Arg393Gln)	ZBTB42 (R393Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494793	NM_001137601.3(ZBTB42):c.584G>A (p.Gly195Asp)	ZBTB42 (G195D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492824	NM_001137601.3(ZBTB42):c.1052G>A (p.Arg351Lys)	ZBTB42 (R351K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483358	NM_001137601.3(ZBTB42):c.1093G>C (p.Val365Leu)	ZBTB42 (V365L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477559	NM_001137601.3(ZBTB42):c.259C>T (p.Arg87Cys)	ZBTB42 (R87C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469992	NM_001137601.3(ZBTB42):c.472A>C (p.Lys158Gln)	ZBTB42 (K158Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458135	NM_001137601.3(ZBTB42):c.638G>T (p.Ser213Ile)	ZBTB42 (S213I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2426765	NC_000014.8:g.(?_105167703)_(105861009_?)del	ADSS1, AHNAK2 +14 more	Deletion	Charcot-Marie-Tooth disease dominant intermediate E +1 more	GUncertain significance
Select item 2425306	NC_000014.8:g.(?_105258915)_(105268803_?)dup	AKT1, ZBTB42	Duplication	Cowden syndrome 6	GUncertain significance
Select item 2424156	NC_000014.8:g.(?_102228231)_(105861009_?)dup	ADSS1, AHNAK2 +47 more	Duplication	Charcot-Marie-Tooth disease axonal type 2O	GUncertain significance
Select item 2424155	NC_000014.8:g.(?_102442029)_(105861009_?)del	ADSS1, AHNAK2 +46 more	Deletion	Charcot-Marie-Tooth disease axonal type 2O	GUncertain significance
Select item 2412235	NM_001137601.3(ZBTB42):c.1115A>T (p.Gln372Leu)	ZBTB42 (Q372L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397202	NM_001137601.3(ZBTB42):c.826C>T (p.Leu276Phe)	ZBTB42 (L276F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396947	NM_001137601.3(ZBTB42):c.976C>T (p.Arg326Trp)	ZBTB42 (R326W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386340	NM_001137601.3(ZBTB42):c.391G>A (p.Ala131Thr)	ZBTB42 (A131T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357070	NM_001137601.3(ZBTB42):c.1004C>T (p.Thr335Ile)	ZBTB42 (T335I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348438	NM_001137601.3(ZBTB42):c.611C>T (p.Pro204Leu)	ZBTB42 (P204L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344513	NM_001137601.3(ZBTB42):c.848G>A (p.Ser283Asn)	ZBTB42 (S283N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341493	NM_001137601.3(ZBTB42):c.1010C>T (p.Pro337Leu)	ZBTB42 (P337L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329842	NM_001137601.3(ZBTB42):c.1061G>T (p.Arg354Leu)	ZBTB42 (R354L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325497	NM_001137601.3(ZBTB42):c.310T>C (p.Tyr104His)	ZBTB42 (Y104H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225381	NM_001137601.3(ZBTB42):c.127G>C (p.Ala43Pro)	ZBTB42 (A43P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1807775	GRCh37/hg19 14q31.2-32.33(chr14:84537502-107285437)x3	ADSS1, AHNAK2 +185 more	Copy number gain	not provided	GPathogenic
Select item 1707441	GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2	ABCD4, ABHD12B +447 more	Copy number gain	See cases	GPathogenic
Select item 1681847	NC_000014.8:g.(?_103336539)_(105861009_?)dup	ATP5MJ, BAG5 +37 more	Duplication	not provided	GUncertain significance
Select item 1526437	GRCh37/hg19 14q32.31-32.33(chr14:101732158-107285437)	SIVA1, TDRD9 +67 more	Copy number loss	not specified	GPathogenic
Select item 1410807	NC_000014.8:g.(?_102229222)_(105861009_?)dup	ADSS1, AHNAK2 +47 more	Duplication	not provided	GUncertain significance
Select item 1341203	GRCh37/hg19 14q32.31-32.33(chr14:101593860-106160500)x1	ADSS1, AHNAK2 +60 more	Copy number loss	not provided	GPathogenic
Select item 1280943	NM_001137601.3(ZBTB42):c.1167G>A (p.Pro389=)	ZBTB42	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1266544	NM_001137601.3(ZBTB42):c.400G>A (p.Ala134Thr)	ZBTB42 (A134T)	Single nucleotide variant (missense variant)	ZBTB42-related condition +1 more	GBenign
Select item 1260467	NM_001137601.3(ZBTB42):c.570G>A (p.Leu190=)	ZBTB42	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1246843	NM_001137601.3(ZBTB42):c.45A>G (p.Arg15=)	ZBTB42	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1031875	NM_001137601.3(ZBTB42):c.1088C>G (p.Thr363Arg)	ZBTB42 (T363R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 980626	GRCh37/hg19 14q32.33(chr14:105204147-105543486)x3	ZBTB42, CLBA1 +8 more	Copy number gain	not provided	GUncertain significance
Select item 980625	GRCh37/hg19 14q32.31-32.33(chr14:102615953-107285437)x1	IGHV3-23, IGHM +62 more	Copy number loss	not provided	GPathogenic
Select item 979404	GRCh37/hg19 14q32.33(chr14:105112467-105285280)x3	INF2, SIVA1 +3 more	Copy number gain	not provided	GUncertain significance
Select item 929832	GRCh37/hg19 14q32.2-32.33(chr14:96829290-107287663)x1	PPP2R5C, RCOR1 +112 more	Copy number loss	See cases	GPathogenic
Select item 831735	NC_000014.9:g.(?_104677659)_(104957672_?)del	ADSS1, AHNAK2 +6 more	Deletion	not provided	GPathogenic
Select item 815682	GRCh37/hg19 14q32.33(chr14:104764078-107285437)x1	CLBA1, CRIP1 +34 more	Copy number loss	not provided	GPathogenic
Select item 815679	GRCh37/hg19 14q32.31-32.33(chr14:103153637-107285437)x1	CEP170B, BAG5 +56 more	Copy number loss	not provided	GPathogenic
Select item 803053	NM_001137601.3(ZBTB42):c.694G>A (p.Glu232Lys)	ZBTB42 (E232K)	Single nucleotide variant (missense variant)	Lethal congenital contracture syndrome 6 +1 more	GBenign
Select item 789824	NM_001137601.3(ZBTB42):c.977G>A (p.Arg326Gln)	ZBTB42 (R326Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 780159	NM_001137601.3(ZBTB42):c.1206C>T (p.Ser402=)	ZBTB42	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 768678	NM_001137601.3(ZBTB42):c.1224C>T (p.His408=)	ZBTB42	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 746127	NM_001137601.3(ZBTB42):c.966C>T (p.Ser322=)	ZBTB42	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 741991	NM_001137601.3(ZBTB42):c.204C>T (p.Gly68=)	ZBTB42	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 688581	GRCh37/hg19 14q32.2-32.33(chr14:99794230-107285437)x3	ADSS1, AHNAK2 +104 more	Copy number gain	not provided	GPathogenic
Select item 687996	GRCh37/hg19 14q32.12-32.33(chr14:91969028-107285437)x3	BTBD6, MIR369 +164 more	Copy number gain	not provided	GPathogenic
Select item 687726	GRCh37/hg19 14q32.31-32.33(chr14:101627916-107147698)x1	ADSS1, AHNAK2 +67 more	Copy number loss	not provided	GPathogenic
Select item 687600	GRCh37/hg19 14q32.33(chr14:105067651-107285437)x1	ADSS1, AHNAK2 +33 more	Copy number loss	not provided	GUncertain significance
Select item 686480	GRCh37/hg19 14q32.31-32.33(chr14:102931119-107285437)x1	ADSS1, AHNAK2 +58 more	Copy number loss	not provided	GPathogenic
Select item 625744	GRCh37/hg19 14q32.2-32.33(chr14:100575917-107281934)	ADSS1, AHNAK2 +98 more	Copy number gain	not provided	GPathogenic
Select item 625708	GRCh37/hg19 14q32.32-32.33(chr14:103804791-105677579)	INF2, JAG2 +30 more	Copy number loss	not provided	GLikely pathogenic
Select item 564134	GRCh37/hg19 14q32.31-32.33(chr14:102191861-106019451)x3	AMN, TEX22 +53 more	Copy number gain	not provided	GPathogenic
Select item 522771	NM_001137601.3(ZBTB42):c.1031C>T (p.Ser344Leu)	ZBTB42 (S344L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 443977	GRCh37/hg19 14q11.2-32.33(chr14:20511673-107285437)	ABCD4, ABHD12B +624 more	Copy number gain	See cases	GPathogenic
Select item 443644	GRCh37/hg19 14q32.2-32.33(chr14:100661319-107285437)x1	ADSS1, AHNAK2 +96 more	Copy number loss	See cases	GPathogenic
Select item 443538	GRCh37/hg19 14q32.33(chr14:104915608-107285437)x1	ADSS1, AHNAK2 +34 more	Copy number loss	See cases	GPathogenic
Select item 443301	GRCh37/hg19 14q32.32-32.33(chr14:103965059-107285437)x1	ADSS1, AHNAK2 +49 more	Copy number loss	See cases	GPathogenic
Select item 442718	GRCh37/hg19 14q24.2-32.33(chr14:73750741-107285437)x3	ABCD4, ACOT1 +261 more	Copy number gain	See cases	GPathogenic
Select item 442421	GRCh37/hg19 14q32.31-32.33(chr14:103153637-107285437)x1	PLD4, PPP1R13B +56 more	Copy number loss	See cases	GPathogenic
Select item 441703	GRCh37/hg19 14q32.31-32.33(chr14:102670706-107285437)x1	ADSS1, AHNAK2 +62 more	Copy number loss	See cases	GPathogenic
Select item 395470	GRCh37/hg19 14q11.2-32.33(chr14:19794561-107234280)x3	ACTN1, ACTR10 +635 more	Copy number gain	See cases	GPathogenic
Select item 253728	GRCh37/hg19 14q32.33(chr14:105259639-105523673)x1	CDCA4, ZBTB42 +6 more	Copy number loss	See cases	GUncertain significance
Select item 221344	chr14:104643721..105932775 complex variant	PACS2, PLD4 +19 more	Complex	Breast ductal adenocarcinoma	GUncertain significance
Select item 183176	NM_001137601.3(ZBTB42):c.1190G>A (p.Arg397His)	ZBTB42 (R397H)	Single nucleotide variant (missense variant)	Lethal congenital contracture syndrome 6	GUncertain significance
Select item 155595	GRCh38/hg38 14q32.2-32.33(chr14:100582059-106877229)x1	PPP2R5C, RCOR1 +571 more	Copy number loss	See cases	GPathogenic
Select item 155306	GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	LOC126861920, LOC126861921 +3280 more	Copy number gain	See cases	GPathogenic
Select item 155087	GRCh38/hg38 14q32.31-32.33(chr14:102605096-106879298)x1	C14orf180, CDC42BPB +367 more	Copy number loss	See cases	GPathogenic
Select item 154736	GRCh38/hg38 14q32.33(chr14:103823600-106879298)x1	ADSS1, AHNAK2 +256 more	Copy number loss	See cases	GPathogenic
Select item 154526	GRCh38/hg38 14q32.32-32.33(chr14:103322414-106855263)x3	BTBD6, C14orf180 +304 more	Copy number gain	See cases	GPathogenic
Select item 154386	GRCh38/hg38 14q32.31-32.33(chr14:101665602-106855263)x1	ADSS1, AHNAK2 +441 more	Copy number loss	See cases	GPathogenic
Select item 154247	GRCh38/hg38 14q32.33(chr14:104051258-106877229)x1	ADSS1, AHNAK2 +241 more	Copy number loss	See cases	GPathogenic
Select item 153602	GRCh38/hg38 14q32.31-32.33(chr14:102239422-106877229)x1	IGHV3-38, IGHV3-43 +397 more	Copy number loss	See cases	GPathogenic
Select item 150835	GRCh38/hg38 14q32.31-32.33(chr14:101925670-106876323)x1	LOC130056610, LOC130056611 +416 more	Copy number loss	See cases	GPathogenic
Select item 149176	GRCh38/hg38 14q24.3-32.33(chr14:77222795-106879298)x3	ADCK1, ADSS1 +1202 more	Copy number gain	See cases	GPathogenic
Select item 146793	GRCh38/hg38 14q32.13-32.33(chr14:95524407-106879501)x1	SNORD114-11, SNORD114-12 +754 more	Copy number loss	See cases	GPathogenic
Select item 146638	GRCh38/hg38 14q32.12-32.33(chr14:92540983-104863658)x3	ZFYVE21, ZNF839 +662 more	Copy number gain	See cases	GPathogenic
Select item 146615	GRCh38/hg38 14q32.2-32.33(chr14:99448012-106850609)x3	ADSS1, AHNAK2 +653 more	Copy number gain	See cases	GPathogenic
Select item 146500	GRCh38/hg38 14q32.33(chr14:104622881-106678844)x1	ADSS1, AHNAK2 +216 more	Copy number loss	See cases	GUncertain significance
Select item 146230	GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	GSC, GSC-DT +3275 more	Copy number gain	See cases	GPathogenic

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