GUK1[gene] - ClinVar

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Items: 64

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155660	GRCh38/hg38 1q32.2-44(chr1:207346642-248930485)x3	ABCB10, ACBD3 +1428 more	Copy number gain	See cases	GPathogenic
Select item 1809607	GRCh38/hg38 1q32.2-42.13(chr1:228006998-228061271)x2	LOC126806029, LOC129932471 +720 more	Copy number loss	Orofacial cleft 2	Gassociation
Select item 58116	GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3	LOC120908923, LOC120947224 +1352 more	Copy number gain	See cases	GPathogenic
Select item 145652	GRCh38/hg38 1q32.2-44(chr1:209963625-248918469)x3	ABCB10, ACBD3 +1326 more	Copy number gain	See cases	GPathogenic
Select item 57302	GRCh38/hg38 1q32.3-44(chr1:214023812-248918469)x3	LOC129932855, LOC129932856 +1168 more	Copy number gain	See cases	GPathogenic
Select item 147449	GRCh38/hg38 1q41-42.13(chr1:223347693-228556332)x1	ACBD3, ACBD3-AS1 +287 more	Copy number loss	See cases	GPathogenic
Select item 57010	GRCh38/hg38 1q41-44(chr1:223347693-248918469)x3	TARBP1, TBCE +968 more	Copy number gain	See cases	GPathogenic
Select item 146575	GRCh38/hg38 1q41-44(chr1:223815147-248918469)x3	LINC02765, LINC02768 +955 more	Copy number gain	See cases	GPathogenic
Select item 58133	GRCh38/hg38 1q41-44(chr1:223828500-248891309)x3	LOC440742, LYPD8 +955 more	Copy number gain	See cases	GPathogenic
Select item 58135	GRCh38/hg38 1q41-44(chr1:223887780-248891309)x3	ABCB10, ACBD3 +953 more	Copy number gain	See cases	GPathogenic
Select item 148701	GRCh38/hg38 1q42.11-44(chr1:224022862-248918469)x3	LOC129932825, LOC129932826 +952 more	Copy number gain	See cases	GPathogenic
Select item 58137	GRCh38/hg38 1q42.11-44(chr1:224096488-248918469)x3	LOC129932658, LOC129932659 +950 more	Copy number gain	See cases	GPathogenic
Select item 155156	GRCh38/hg38 1q42.12-42.13(chr1:225382172-230418801)x1	ABCB10, ACBD3 +309 more	Copy number loss	See cases	GPathogenic
Select item 154381	GRCh38/hg38 1q42.12-44(chr1:225438480-248787200)x3	LOC126806053, LOC126806054 +870 more	Copy number gain	See cases	GPathogenic
Select item 146517	GRCh38/hg38 1q42.12-42.2(chr1:226185124-232872488)x1	ABCB10, ACBD3 +313 more	Copy number loss	See cases	GPathogenic
Select item 145605	GRCh38/hg38 1q42.13(chr1:227613596-229249335)x4	ARF1, BTNL10 +100 more	Copy number gain	See cases	GLikely pathogenic
Select item 3103336	NM_001159390.2(GUK1):c.20C>G (p.Ala7Gly)	GUK1, LOC129932713 (A7G)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2494209	NM_001159390.2(GUK1):c.23G>T (p.Gly8Val)	GUK1, LOC129932713 (G8V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2303262	NM_001159390.2(GUK1):c.53C>T (p.Pro18Leu)	GUK1, LOC129932713 (P18L)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2489378	NM_001159390.2(GUK1):c.199G>C (p.Gly67Arg)	GUK1 (G67R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283185	NM_001159390.2(GUK1):c.277G>A (p.Glu93Lys)	GUK1 (E72K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103337	NM_001159390.2(GUK1):c.300C>A (p.Asn100Lys)	GUK1 (N79K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103338	NM_001159390.2(GUK1):c.350G>A (p.Arg117His)	GUK1 (R117H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394379	NM_001159390.2(GUK1):c.358G>A (p.Val120Met)	GUK1 (V120M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103339	NM_001159390.2(GUK1):c.367G>A (p.Val123Met)	GUK1 (V102M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389022	NM_001159390.2(GUK1):c.382G>A (p.Val128Met)	GUK1 (V107M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244450	NM_001159390.2(GUK1):c.404A>T (p.Asp135Val)	GUK1 (D114V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354945	NM_001159390.2(GUK1):c.461G>A (p.Arg154Gln)	GUK1 (R133Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224934	NM_001159390.2(GUK1):c.499G>T (p.Val167Leu)	GUK1 (V146L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229055	NM_001159390.2(GUK1):c.506G>A (p.Arg169Gln)	GUK1 (R148Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302139	NM_001159390.2(GUK1):c.530T>C (p.Met177Thr)	GUK1 (M156T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 221378	GRCh38/hg38 1q42.13(chr1:228148416-228372055)x1	GJC2, GUK1 +7 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 2369291	NM_001159390.2(GUK1):c.633G>C (p.Lys211Asn)	GUK1 (K190N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311306	NM_001159390.2(GUK1):c.649G>A (p.Gly217Ser)	GUK1 (G196S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409220	NM_001159390.2(GUK1):c.*19G>A	GUK1 (R197Q)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2386080	NM_001159390.2(GUK1):c.*27G>C	GUK1 (G200R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2542778	NM_001159390.2(GUK1):c.*133G>A	GUK1 (C235Y)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3247647	NC_000001.10:g.(?_228194830)_(228566496_?)del	ARF1, C1orf35 +6 more	Deletion	Spastic paraplegia +2 more	GPathogenic
Select item 3062877	GRCh37/hg19 1q42.13(chr1:228215364-229747702)x1	CCSAP, ABCB10 +21 more	Copy number loss	not specified	GPathogenic
Select item 1810315	GRCh37/hg19 1q42.11-43(chr1:224230307-243181599)x3	ABCB10, ACBD3 +113 more	Copy number gain	not provided	Gnot provided
Select item 1809372	GRCh37/hg19 1q41-44(chr1:223972939-249224684)x3	ABCB10, ACBD3 +185 more	Copy number gain	not provided	GPathogenic
Select item 1809265	GRCh37/hg19 1q42.13-43(chr1:227992928-236659905)x3	ABCB10, ACTA1 +65 more	Copy number gain	not provided	GLikely pathogenic
Select item 1708464	GRCh37/hg19 1q31.3-44(chr1:197867914-249224684)x3	COA6, COG2 +381 more	Copy number gain	See cases	GPathogenic
Select item 1527603	GRCh37/hg19 1q42.13-42.2(chr1:228214912-231483538)	ABCB10, ACTA1 +36 more	Copy number loss	not specified	GPathogenic
Select item 1527592	GRCh37/hg19 1q42.12-42.2(chr1:226131690-231908227)	ABCB10, ACBD3 +55 more	Copy number loss	not specified	GLikely pathogenic
Select item 1412630	NC_000001.10:g.(?_228194830)_(228566496_?)dup	ARF1, C1orf35 +6 more	Duplication	Multiple mitochondrial dysfunctions syndrome 3 +1 more	GUncertain significance
Select item 1328448	GRCh37/hg19 1q42.13(chr1:227782268-229506509)x1	ARF1, BTNL10 +22 more	Copy number loss	not provided	GUncertain significance
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	FCGR3A, LCE3C +956 more	Duplication	Parathyroid carcinoma +2 more	GUncertain significance
Select item 929379	GRCh37/hg19 1q32.2-44(chr1:210152794-249218992)x3	CHML, CHRM3 +250 more	Copy number gain	See cases	GPathogenic
Select item 816482	GRCh37/hg19 1q32.1-44(chr1:204045948-249218992)x3	C1orf35, C1orf74 +320 more	Copy number gain	See cases	GPathogenic
Select item 814168	GRCh37/hg19 1q41-42.2(chr1:223653722-234591807)x1	FBXO28, ACBD3 +83 more	Copy number loss	not provided	GPathogenic
Select item 814163	GRCh37/hg19 1q41-43(chr1:219916966-239004378)x3	CCDC185, NTPCR +127 more	Copy number gain	not provided	GPathogenic
Select item 687403	GRCh37/hg19 1q42.13(chr1:228235107-228983659)x3	ARF1, BTNL10 +14 more	Copy number gain	not provided	GUncertain significance
Select item 685144	GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3	C4BPB, CACNA1S +433 more	Copy number gain	not provided	GPathogenic
Select item 590949	GRCh37/hg19 1q42.13(chr1:228297613-228703236)	GUK1, H2AC25 +14 more	Copy number gain	Aortic valve disease 1	GUncertain significance
Select item 565231	GRCh37/hg19 1q42.13(chr1:227696109-229152386)x3	ARF1, GJC2 +19 more	Copy number gain	not provided	GLikely pathogenic
Select item 565225	GRCh37/hg19 1q41-44(chr1:218252551-249224684)x3	H2BC26, H3-3A +213 more	Copy number gain	not provided	GPathogenic
Select item 442387	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	CD34, CD46 +2014 more	Copy number gain	See cases	GPathogenic
Select item 442386	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	GPATCH2, GPATCH3 +2014 more	Copy number gain	See cases	GPathogenic
Select item 442184	GRCh37/hg19 1q42.13(chr1:227774916-228335196)x3	ARF1, C1orf35 +8 more	Copy number gain	See cases	GUncertain significance
Select item 441866	GRCh37/hg19 1q42.11-44(chr1:224105294-249224684)x3	ABCB10, ACBD3 +184 more	Copy number gain	See cases	GPathogenic
Select item 394081	GRCh37/hg19 1q31.3-44(chr1:195483439-249213000)x3	AVPR1B, B3GALNT2 +393 more	Copy number gain	See cases	GPathogenic
Select item 253906	GRCh37/hg19 1q42.12-42.13(chr1:226871745-229906954)x1	GJC2, TRIM17 +31 more	Copy number loss	See cases	GUncertain significance
Select item 253654	GRCh37/hg19 1q31.3-42.13(chr1:197811907-228997888)x3	ACBD3, ADIPOR1 +242 more	Copy number gain	See cases	GPathogenic

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Items: 64