ClinVar for Gene (Select 2650) - ClinVar

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Links from Gene

Items: 66

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3281063	NM_001490.5(GCNT1):c.485A>G (p.Tyr162Cys)	GCNT1 (Y162C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3281062	NM_001490.5(GCNT1):c.1087G>A (p.Val363Ile)	GCNT1 (V363I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099123	NM_001490.5(GCNT1):c.667A>G (p.Ile223Val)	GCNT1 (I223V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099121	NM_001490.5(GCNT1):c.184G>A (p.Val62Ile)	GCNT1 (V62I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3099120	NM_001490.5(GCNT1):c.164G>A (p.Ser55Asn)	GCNT1 (S55N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099119	NM_001490.5(GCNT1):c.1249C>T (p.His417Tyr)	GCNT1 (H417Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099118	NM_001490.5(GCNT1):c.1159G>A (p.Asp387Asn)	GCNT1 (D387N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3099117	NM_001490.5(GCNT1):c.1025A>G (p.Tyr342Cys)	GCNT1 (Y342C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	DMAC1, DMRT1 +769 more	Copy number gain	not specified	GPathogenic
Select item 2659259	NM_001490.5(GCNT1):c.795G>A (p.Lys265=)	GCNT1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2550819	NM_001490.5(GCNT1):c.1213G>T (p.Asp405Tyr)	GCNT1 (D405Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548337	NM_001490.5(GCNT1):c.379A>C (p.Ile127Leu)	GCNT1 (I127L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517848	NM_001490.5(GCNT1):c.319C>T (p.Arg107Cys)	GCNT1 (R107C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513845	NM_001490.5(GCNT1):c.574C>T (p.Arg192Trp)	GCNT1 (R192W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474796	NM_001490.5(GCNT1):c.361T>C (p.Phe121Leu)	GCNT1 (F121L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464874	NM_001490.5(GCNT1):c.1168T>C (p.Trp390Arg)	GCNT1 (W390R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460059	NM_001490.5(GCNT1):c.127G>T (p.Val43Phe)	GCNT1 (V43F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378623	NM_001490.5(GCNT1):c.91G>A (p.Val31Ile)	GCNT1 (V31I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295195	NM_001490.5(GCNT1):c.554T>C (p.Val185Ala)	GCNT1 (V185A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294452	NM_001490.5(GCNT1):c.538A>C (p.Ser180Arg)	GCNT1 (S180R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293376	NM_001490.5(GCNT1):c.1115G>A (p.Cys372Tyr)	GCNT1 (C372Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260094	NM_001490.5(GCNT1):c.20G>A (p.Arg7Gln)	GCNT1 (R7Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233587	NM_001490.5(GCNT1):c.43A>C (p.Thr15Pro)	GCNT1 (T15P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205656	NM_001490.5(GCNT1):c.388C>A (p.His130Asn)	GCNT1 (H130N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1711101	GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3	ADAMTSL1, CEP78 +596 more	Copy number gain	See cases	GPathogenic
Select item 1703688	GRCh37/hg19 9p22.1-q33.1(chr9:19356861-119513311)	ATOSB, ATP6V1G1 +417 more	Copy number loss	Distal tetrasomy 15q	GUncertain significance
Select item 1527524	GRCh37/hg19 9q21.13-21.2(chr9:78824128-79392249)	GCNT1, PCA3 +3 more	Copy number gain	not specified	GUncertain significance
Select item 1527521	GRCh37/hg19 9q21.11-33.2(chr9:71349994-122603410)	ABCA1, ABHD17B +261 more	Copy number gain	not specified	GLikely pathogenic
Select item 1527491	GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389)	ANKRD18A, ANKRD18B +768 more	Copy number gain	not specified	GPathogenic
Select item 1527488	GRCh37/hg19 9p24.3-q21.32(chr9:203861-84155399)	SPATA31A5, SPATA31A6 +257 more	Copy number gain	not specified	GPathogenic
Select item 733713	NM_001490.5(GCNT1):c.703T>C (p.Leu235=)	GCNT1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 694460	NC_000009.11:g.12246100_101559378inv	ANKS6, ANP32B +326 more	Inversion	Abnormal chromosome morphology +1 more	GLikely pathogenic
Select item 688286	GRCh37/hg19 9q21.13(chr9:78787760-79180790)x3	GCNT1, PCSK5 +1 more	Copy number gain	not provided	GUncertain significance
Select item 687864	GRCh37/hg19 9q21.13-21.31(chr9:78672613-83349616)x1	CEP78, FOXB2 +10 more	Copy number loss	not provided	GUncertain significance
Select item 687100	GRCh37/hg19 9q21.11-34.3(chr9:71416475-141020389)x3	AMBP, ANAPC2 +552 more	Copy number gain	not provided	GPathogenic
Select item 685659	GRCh37/hg19 9q21.11-21.31(chr9:70974661-81829792)x1	ABHD17B, ALDH1A1 +42 more	Copy number loss	not provided	GPathogenic
Select item 685192	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3	MSMP, OR13D1 +769 more	Copy number gain	not provided	GPathogenic
Select item 617751	Single allele	APBA1, APTX +185 more	Complex	Glioma	GLikely pathogenic
Select item 563680	GRCh37/hg19 9q21.11-21.32(chr9:68999534-84656998)x1	ABHD17B, ALDH1A1 +54 more	Copy number loss	not provided	GPathogenic
Select item 563676	GRCh37/hg19 9q21.13-21.31(chr9:74534790-84014155)x1	ALDH1A1, ANXA1 +24 more	Copy number loss	not provided	GPathogenic
Select item 523294	GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928)	ANGPTL2, ANKS6 +555 more	Copy number gain	Seizure +2 more	GLikely pathogenic
Select item 443986	GRCh37/hg19 9p24.3-q34.3(chr9:203862-141020389)	ODF2, OGN +769 more	Copy number gain	See cases	GPathogenic
Select item 442687	GRCh37/hg19 9q21.11-21.31(chr9:68734571-83557267)x3	ABHD17B, ALDH1A1 +50 more	Copy number gain	See cases	GPathogenic
Select item 442489	GRCh37/hg19 9p24.3-q21.33(chr9:203861-88189913)x3	ABHD17B, ACER2 +274 more	Copy number gain	See cases	GPathogenic
Select item 441960	GRCh37/hg19 9q21.13-21.2(chr9:78210974-79206408)x1	GCNT1, PCSK5 +1 more	Copy number loss	See cases	GUncertain significance
Select item 441750	GRCh37/hg19 9q21.11-22.1(chr9:70966262-90761254)x4	ABHD17B, AGTPBP1 +74 more	Copy number gain	See cases	GPathogenic
Select item 395707	GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC124210612, LOC124210613 +3786 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 155038	GRCh38/hg38 9q21.13-21.2(chr9:76235414-76751538)x3	GCNT1, LOC113839560 +19 more	Copy number gain	See cases	GUncertain significance
Select item 154945	GRCh38/hg38 9p24.3-q21.31(chr9:193412-79877816)x3	CDKN2B, CDKN2B-AS1 +1214 more	Copy number gain	See cases	GPathogenic
Select item 153561	GRCh38/hg38 9p24.3-q22.1(chr9:203861-88130444)x4	LOC130001854, LOC130001855 +1367 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC113839542, LOC113839543 +3786 more	Copy number gain	See cases	GPathogenic
Select item 151006	GRCh38/hg38 9q21.12-31.3(chr9:69627642-111454304)x3	ABCA1, ABHD17B +1188 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	LOC121331326, LOC121331327 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC126860737, LOC126860738 +3786 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	ABCA1, ABCA2 +3786 more	Copy number gain	See cases	GPathogenic
Select item 148903	GRCh38/hg38 9q21.13-21.2(chr9:76127281-76968483)x1	GCNT1, LOC113839560 +24 more	Copy number loss	See cases	GUncertain significance
Select item 148901	GRCh38/hg38 9q21.11-21.32(chr9:68499530-83670227)x1	LOC130001938, LOC130001939 +263 more	Copy number loss	See cases	GPathogenic
Select item 147624	GRCh38/hg38 9q21.11-31.2(chr9:68420430-106579493)x3	ABCA1, ABHD17B +1072 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC130002189, LOC130002190 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC110121197, LOC110121234 +3786 more	Copy number gain	See cases	GPathogenic
Select item 59109	GRCh38/hg38 9q21.13-21.31(chr9:73706686-80370629)x1	C9orf40, CARNMT1 +102 more	Copy number loss	See cases	GPathogenic
Select item 59108	GRCh38/hg38 9q21.13-21.2(chr9:72224348-77332127)x1	ALDH1A1, ANXA1 +90 more	Copy number loss	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC121331342, LOC121331343 +3786 more	Copy number gain	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 66