TRABD[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144164	GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3	IL17RA, LINC01640 +2088 more	Copy number gain	See cases	GPathogenic
Select item 145336	GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3	LOC130067403, LOC130067404 +2088 more	Copy number gain	See cases	GPathogenic
Select item 57942	GRCh38/hg38 22q12.3-13.33(chr22:37061769-50738932)x3	LOC130067651, LOC130067652 +1004 more	Copy number gain	See cases	GPathogenic
Select item 145111	GRCh38/hg38 22q13.1-13.33(chr22:40202014-50735806)x3	LOC130067596, LOC130067597 +687 more	Copy number gain	See cases	GPathogenic
Select item 147775	GRCh38/hg38 22q13.2-13.33(chr22:41871143-50739836)x1	A4GALT, ACR +580 more	Copy number loss	See cases	GPathogenic
Select item 154688	GRCh38/hg38 22q13.2-13.33(chr22:42080077-50739836)x3	LOC126863184, LOC126863185 +541 more	Copy number gain	See cases	GPathogenic
Select item 153178	GRCh38/hg38 22q13.2-13.33(chr22:42380961-50759410)x3	LOC126863187, LOC126863188 +523 more	Copy number gain	See cases	GPathogenic
Select item 57636	GRCh38/hg38 22q13.2-13.33(chr22:42433752-50738932)x1	A4GALT, ACR +521 more	Copy number loss	See cases	GPathogenic
Select item 147622	GRCh38/hg38 22q13.2-13.33(chr22:42493445-50268479)x1	A4GALT, ALG12 +428 more	Copy number loss	See cases	GPathogenic
Select item 57944	GRCh38/hg38 22q13.2-13.33(chr22:42599757-50725241)x3	A4GALT, ADM2 +502 more	Copy number gain	See cases	GPathogenic
Select item 57945	GRCh38/hg38 22q13.2-13.33(chr22:42653747-50739836)x3	LOC126863187, LOC126863188 +495 more	Copy number gain	See cases	GPathogenic
Select item 148050	GRCh38/hg38 22q13.2-13.33(chr22:42710276-50739836)x3	CIMAP1B, CPT1B +492 more	Copy number gain	See cases	GPathogenic
Select item 57669	GRCh38/hg38 22q13.2-13.33(chr22:42826246-50739836)x1	LOC130067640, LOC130067641 +483 more	Copy number loss	See cases	GPathogenic
Select item 152914	GRCh38/hg38 22q13.2-13.33(chr22:42837094-50735806)x1	ADM2, ALG12 +481 more	Copy number loss	See cases	GPathogenic
Select item 976862	NC_000022.11:g.43032129_50739836del	CRELD2, DENND6B +471 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 152340	GRCh38/hg38 22q13.2-13.33(chr22:43187980-50745444)x1	ACR, ADM2 +451 more	Copy number loss	See cases	GPathogenic
Select item 976870	NC_000022.11:g.43802117_50806121del	DENND6B, EFCAB6 +443 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 57670	GRCh38/hg38 22q13.31-13.33(chr22:43807366-50739836)x1	ACR, ADM2 +441 more	Copy number loss	See cases	GPathogenic
Select item 146121	GRCh38/hg38 22q13.31-13.33(chr22:43902561-50739836)x1	ACR, ADM2 +434 more	Copy number loss	See cases	GPathogenic
Select item 146895	GRCh38/hg38 22q13.31-13.33(chr22:43992879-50683114)x3	ADM2, ALG12 +428 more	Copy number gain	See cases	GBenign
Select item 976875	NC_000022.11:g.44245760_50806121del	LOC121627953, LOC121627954 +411 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 3062348	GRCh38/hg38 22q13.31-13.33(chr22:44549957-50789329)	CHKB, LOC112695108 +404 more	Copy number loss	Phelan-McDermid syndrome	GPathogenic
Select item 144383	GRCh38/hg38 22q13.31-13.33(chr22:44606363-50739836)x1	ACR, ADM2 +401 more	Copy number loss	See cases	GPathogenic
Select item 976876	NC_000022.11:g.44702479_50806138del	CPT1B, CRELD2 +401 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 57672	GRCh38/hg38 22q13.31-13.33(chr22:44740175-50739836)x1	ACR, ADM2 +396 more	Copy number loss	See cases	GPathogenic
Select item 147743	GRCh38/hg38 22q13.31-13.33(chr22:44764289-50739836)x1	ACR, ADM2 +396 more	Copy number loss	See cases	GPathogenic
Select item 147377	GRCh38/hg38 22q13.31-13.33(chr22:44797239-50739836)x3	ACR, ADM2 +396 more	Copy number gain	See cases	GPathogenic
Select item 57947	GRCh38/hg38 22q13.31-13.33(chr22:44811200-50739836)x3	LOC130067697, LOC130067698 +396 more	Copy number gain	See cases	GPathogenic
Select item 57264	GRCh38/hg38 22q13.31-13.33(chr22:45239376-50739836)x1	ACR, ADM2 +371 more	Copy number loss	See cases	GPathogenic
Select item 57673	GRCh38/hg38 22q13.31-13.33(chr22:45648256-50739836)x1	ACR, ADM2 +343 more	Copy number loss	See cases	GPathogenic
Select item 976865	NC_000022.11:g.45708330_50737364del	TRABD, TRABD-AS1 +338 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 976872	NC_000022.11:g.45819932_50737806del	ADM2, ALG12 +333 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 57398	GRCh38/hg38 22q13.31-13.33(chr22:46065705-50739836)x1	ACR, ADM2 +315 more	Copy number loss	See cases	GPathogenic
Select item 976864	NC_000022.11:g.46269281_50740560del	ACR, ADM2 +295 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 155420	GRCh38/hg38 22q13.31-13.33(chr22:46361165-50759299)x1	LOC130067809, LOC130067810 +288 more	Copy number loss	See cases	GPathogenic
Select item 976873	NC_000022.11:g.46467175_50759338del	LOC130067779, LOC130067780 +281 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 976869	NC_000022.11:g.46489644_50806138del	LOC126863185, LOC126863186 +282 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 152137	GRCh38/hg38 22q13.31-13.33(chr22:46732445-50780522)x1	ACR, ADM2 +260 more	Copy number loss	See cases	GPathogenic
Select item 146310	GRCh38/hg38 22q13.31-13.33(chr22:46919818-50739836)x1	LOC130067846, LOC130067847 +240 more	Copy number loss	See cases	GPathogenic
Select item 57674	GRCh38/hg38 22q13.31-13.33(chr22:47122613-50739836)x1	LOC126863173, LOC126863174 +235 more	Copy number loss	See cases	GPathogenic
Select item 57675	GRCh38/hg38 22q13.31-13.33(chr22:47234701-50739836)x1	ACR, ADM2 +230 more	Copy number loss	See cases	GPathogenic
Select item 976868	NC_000022.11:g.47447433_50806138del	LOC126863188, LOC129391286 +228 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 976863	NC_000022.11:g.47513236_50806138del	ACR, ADM2 +226 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 976866	NC_000022.11:g.47705262_50739836del	LOC130067774, LOC130067775 +221 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 57193	GRCh38/hg38 22q13.31-13.33(chr22:47705262-50739836)x1	ACR, ADM2 +221 more	Copy number loss	See cases	GPathogenic
Select item 976861	NC_000022.11:g.47823120_50759410del	LOC130067781, LOC130067782 +221 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 57701	GRCh38/hg38 22q13.32-13.33(chr22:48138038-50739836)x1	ACR, ADM2 +211 more	Copy number loss	See cases	GPathogenic
Select item 154522	GRCh38/hg38 22q13.32-13.33(chr22:48241375-50739836)x1	ACR, ADM2 +210 more	Copy number loss	See cases	GPathogenic
Select item 976871	NC_000022.11:g.48500337_50739785del	ACR, ADM2 +206 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 976867	NC_000022.11:g.48500344_50780581del	LOC126863183, LOC126863184 +207 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 148302	GRCh38/hg38 22q13.32-13.33(chr22:48500344-50780581)x1	ACR, ADM2 +207 more	Copy number loss	See cases	GPathogenic
Select item 147807	GRCh38/hg38 22q13.32-13.33(chr22:48614336-50739836)x1	ACR, ADM2 +204 more	Copy number loss	See cases	GPathogenic
Select item 57703	GRCh38/hg38 22q13.32-13.33(chr22:48654672-50739836)x1	ACR, ADM2 +204 more	Copy number loss	See cases	GPathogenic
Select item 976874	NC_000022.11:g.49181210_50759297del	DENND6B, HDAC10 +190 more	Deletion	Phelan-McDermid syndrome	GPathogenic
Select item 144225	GRCh38/hg38 22q13.33(chr22:49315518-50739836)x1	ACR, ADM2 +186 more	Copy number loss	See cases	GPathogenic
Select item 144377	GRCh38/hg38 22q13.33(chr22:49378128-50739836)x1	ACR, ADM2 +185 more	Copy number loss	See cases	GPathogenic
Select item 57704	GRCh38/hg38 22q13.33(chr22:49395349-50738932)x1	ACR, ADM2 +185 more	Copy number loss	See cases	GPathogenic
Select item 146391	GRCh38/hg38 22q13.33(chr22:49504768-50780581)x1	ACR, ADM2 +185 more	Copy number loss	See cases	GPathogenic
Select item 155641	GRCh38/hg38 22q13.33(chr22:49529760-50759410)x1	LOC121853048, LOC125446259 +184 more	Copy number loss	See cases	GPathogenic
Select item 150859	GRCh38/hg38 22q13.33(chr22:49535113-50780581)x1	ACR, ADM2 +185 more	Copy number loss	See cases	GPathogenic
Select item 2579283	GRCh38/hg38 22q13.33(chr22:49757859-50740457)x1	ACR, ADM2 +178 more	Copy number loss	Phelan-McDermid syndrome	GPathogenic
Select item 1703238	Single allele	ACR, LOC130067783 +166 more	Duplication	Chromosome 22q13 duplication syndrome	GPathogenic
Select item 1679643	Single allele	LOC130067853, LOC130067854 +117 more	Duplication	not provided	GUncertain significance
Select item 153101	GRCh38/hg38 22q13.33(chr22:50055231-50202728)x1	LOC125446261, LOC130067807 +24 more	Copy number loss	See cases	GUncertain significance
Select item 146870	GRCh38/hg38 22q13.33(chr22:50055303-50677724)x3	ADM2, ARSA +123 more	Copy number gain	See cases	GUncertain significance
Select item 151373	GRCh38/hg38 22q13.33(chr22:50149563-50780522)x1	ACR, ADM2 +124 more	Copy number loss	See cases	GPathogenic
Select item 152143	GRCh38/hg38 22q13.33(chr22:50180224-50199565)x1	LOC130067819, LOC130067820 +14 more	Copy number loss	See cases	GLikely benign
Select item 2487782	NM_001320485.2(TRABD):c.7G>T (p.Gly3Trp)	TRABD (G3W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457742	NM_001320485.2(TRABD):c.7G>A (p.Gly3Arg)	TRABD (G3R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306394	NM_001320485.2(TRABD):c.31G>A (p.Glu11Lys)	TRABD (E11K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371465	NM_001320485.2(TRABD):c.84G>C (p.Arg28Ser)	TRABD (R28S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462360	NM_001320485.2(TRABD):c.99C>A (p.Asp33Glu)	TRABD (D33E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2465343	NM_001320485.2(TRABD):c.124G>A (p.Ala42Thr)	TRABD (A42T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181724	NM_001320485.2(TRABD):c.167A>G (p.Gln56Arg)	TRABD (Q56R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457754	NM_001320485.2(TRABD):c.169C>T (p.Arg57Trp)	TRABD (R57W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181725	NM_001320485.2(TRABD):c.182C>T (p.Pro61Leu)	TRABD (P61L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257787	NM_001320485.2(TRABD):c.185G>A (p.Arg62His)	TRABD (R62H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181726	NM_001320485.2(TRABD):c.287G>A (p.Arg96Gln)	TRABD (R96Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181727	NM_001320485.2(TRABD):c.313G>A (p.Val105Met)	TRABD (V105M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257081	NM_001320485.2(TRABD):c.400C>G (p.Leu134Val)	TRABD (L134V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619962	NM_001320485.2(TRABD):c.430A>G (p.Met144Val)	TRABD (M144V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353038	NM_001320485.2(TRABD):c.572G>A (p.Arg191Gln)	TRABD (R191Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181728	NM_001320485.2(TRABD):c.724G>A (p.Ala242Thr)	TRABD (A242T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473826	NM_001320485.2(TRABD):c.739G>A (p.Glu247Lys)	TRABD (E247K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462165	NM_001320485.2(TRABD):c.781G>A (p.Val261Ile)	TRABD (V265I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2217789	NM_001320485.2(TRABD):c.796A>G (p.Met266Val)	TRABD (M270V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558404	NM_001320485.2(TRABD):c.815G>A (p.Arg272Gln)	TRABD (R272Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407096	NM_001320485.2(TRABD):c.862G>A (p.Val288Ile)	TRABD (V292I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181730	NM_001320485.2(TRABD):c.957C>T (p.Thr319=)	TRABD	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3181731	NM_001320485.2(TRABD):c.965C>T (p.Pro322Leu)	TRABD (P326L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374591	NM_001320485.2(TRABD):c.968C>T (p.Pro323Leu)	TRABD (P327L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400746	NM_001320485.2(TRABD):c.973G>A (p.Val325Ile)	TRABD (V325I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2219687	NM_001320485.2(TRABD):c.994T>A (p.Leu332Met)	TRABD (L332M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319786	NM_001320485.2(TRABD):c.1042T>C (p.Trp348Arg)	TRABD (W348R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597990	NM_001320485.2(TRABD):c.1048G>A (p.Gly350Ser)	TRABD (G350S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300074	NM_001320485.2(TRABD):c.1061C>T (p.Ala354Val)	TRABD (A358V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2653366	NM_001320485.2(TRABD):c.1083C>T (p.Pro361=)	TRABD	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3181723	NM_001320485.2(TRABD):c.1087G>T (p.Ala363Ser)	TRABD (A363S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3062451	GRCh37/hg19 22q13.2-13.33(chr22:43107363-51156692)x1	A4GALT, ADM2 +78 more	Copy number loss	not specified	GPathogenic
Select item 3062449	GRCh37/hg19 22q13.2-13.33(chr22:44034281-51197838)x1	ACR, ADM2 +69 more	Copy number loss	not specified	GPathogenic

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