TOR2A[gene] - ClinVar

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Items: 74

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 160862	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	LOC130001539, LOC130001540 +3785 more	Copy number gain	See cases	GPathogenic
Select item 150340	GRCh38/hg38 9p11.2-q34.3(chr9:193412-138159073)x3	BSPRY, C5 +3784 more	Copy number gain	See cases	GPathogenic
Select item 150050	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138159073)x3	LOC113839508, LOC113839509 +3785 more	Copy number gain	See cases	GPathogenic
Select item 149828	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138124524)x3	FKBP15, FKTN +3785 more	Copy number gain	See cases	GPathogenic
Select item 59875	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138114463)x3	LOC130001667, LOC130001668 +3785 more	Copy number gain	See cases	GPathogenic
Select item 33205	GRCh38/hg38 9p24.3-q34.3(chr9:193412-138179445)x3	ABCA1, ABCA2 +3785 more	Copy number gain	See cases	GPathogenic
Select item 153518	GRCh38/hg38 9p24.3-q34.3(chr9:203861-138125937)x3	LOC116186942, LOC116186943 +3785 more	Copy number gain	See cases	GPathogenic
Select item 155409	GRCh38/hg38 9p24.3-q34.3(chr9:203862-138125937)x3	ABCA1, ABCA2 +3785 more	Copy number gain	See cases	GPathogenic
Select item 144309	GRCh38/hg38 9p24.3-q34.3(chr9:204193-138179445)	LOC121366033, LOC121366034 +3785 more	Copy number gain	See cases	GPathogenic
Select item 145579	GRCh38/hg38 9q33.2-34.3(chr9:121073102-138179445)x3	ABCA2, ABL1 +1272 more	Copy number gain	See cases	GPathogenic
Select item 57324	GRCh38/hg38 9q33.2-34.3(chr9:121112395-138075224)x3	ABCA2, ABL1 +1268 more	Copy number gain	See cases	GPathogenic
Select item 57353	GRCh38/hg38 9q33.2-34.3(chr9:122792658-138124532)x3	LOC130003132, LOC130003133 +1210 more	Copy number gain	See cases	GPathogenic
Select item 148721	GRCh38/hg38 9q33.3-34.11(chr9:125055865-128637946)x1	AK1, ANGPTL2 +250 more	Copy number loss	See cases	GPathogenic
Select item 59125	GRCh38/hg38 9q33.3-34.11(chr9:125993583-129682375)x1	AK1, ANGPTL2 +309 more	Copy number loss	See cases	GPathogenic
Select item 57204	GRCh38/hg38 9q33.3-34.11(chr9:126081595-127781685)x1	ANGPTL2, CFAP157 +93 more	Copy number loss	See cases	GPathogenic
Select item 663424	NC_000009.11:g.(?_130216797)_(130953151_?)dup	LOC130002656, LOC130002657 +93 more	Duplication	Congenital muscular dystrophy with intellectual disability and severe epilepsy	GUncertain significance
Select item 662282	NC_000009.12:g.(?_127612384)_(128566997_?)del	LOC130002653, LOC130002654 +130 more	Deletion	Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome +1 more	GPathogenic
Select item 3181318	NM_001085347.3(TOR2A):c.958T>C (p.Phe320Leu)	TOR2A (F320L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328117	NM_001085347.3(TOR2A):c.944C>T (p.Ser315Phe)	TOR2A (S153F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207923	NM_001085347.3(TOR2A):c.937G>A (p.Val313Met)	TOR2A (V151M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223199	NM_001085347.3(TOR2A):c.925G>A (p.Gly309Ser)	TOR2A (G309S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 723314	NM_001085347.3(TOR2A):c.907C>A (p.Gln303Lys)	TOR2A (Q141K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3328119	NM_001085347.3(TOR2A):c.825G>A (p.Glu275=)	TOR2A (A233T +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 3328120	NM_001085347.3(TOR2A):c.813C>T (p.Cys271=)	TOR2A (R229C +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 2517156	NM_001085347.3(TOR2A):c.805C>T (p.Arg269Trp)	TOR2A (R269W +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181317	NM_001085347.3(TOR2A):c.801C>T (p.His267=)	TOR2A (R63C +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 2366020	NM_001085347.3(TOR2A):c.785C>G (p.Pro262Arg)	TOR2A (P262R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2568799	NM_001085347.3(TOR2A):c.766G>A (p.Ala256Thr)	TOR2A (A256T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592214	NM_001085347.3(TOR2A):c.765C>T (p.Asp255=)	TOR2A (R213C +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 2276457	NM_001085347.3(TOR2A):c.737C>T (p.Ser246Leu)	TOR2A (S84L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2239204	NM_001085347.3(TOR2A):c.734A>G (p.Asn245Ser)	TOR2A (N245S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2456206	NM_001085347.3(TOR2A):c.697C>T (p.Arg233Cys)	TOR2A (R233C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3181315	NM_001085347.3(TOR2A):c.679C>G (p.Leu227Val)	TOR2A (L227V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2220445	NM_001085347.3(TOR2A):c.656G>C (p.Arg219Pro)	TOR2A (R219P +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2350483	NM_001085347.3(TOR2A):c.646C>T (p.Arg216Trp)	TOR2A (R54W +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3328121	NM_001085347.3(TOR2A):c.623T>C (p.Val208Ala)	TOR2A (V208A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3181314	NM_001085347.3(TOR2A):c.608A>C (p.Lys203Thr)	TOR2A (K41T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2659512	NM_001085347.3(TOR2A):c.593+160G>A	TOR2A	Single nucleotide variant (3 prime UTR variant +2 more)	not provided	GLikely benign
Select item 2323957	NM_001085347.3(TOR2A):c.553T>C (p.Tyr185His)	TOR2A (Y185H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409902	NM_001085347.3(TOR2A):c.463C>T (p.Arg155Cys)	TOR2A (P66L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520688	NM_001085347.3(TOR2A):c.423T>A (p.Asp141Glu)	TOR2A (D141E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181313	NM_001085347.3(TOR2A):c.376G>A (p.Val126Ile)	TOR2A (V126I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181312	NM_001085347.3(TOR2A):c.362A>G (p.His121Arg)	TOR2A (H121R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181311	NM_001085347.3(TOR2A):c.356G>A (p.Arg119His)	TOR2A (R119H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2471104	NM_001085347.3(TOR2A):c.338G>A (p.Gly113Asp)	TOR2A (G113D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226188	NM_001085347.3(TOR2A):c.247C>T (p.Pro83Ser)	TOR2A (P83S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338327	NM_001085347.3(TOR2A):c.194T>C (p.Leu65Pro)	TOR2A (L65P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181310	NM_001085347.3(TOR2A):c.193C>A (p.Leu65Met)	TOR2A (L65M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3181309	NM_001085347.3(TOR2A):c.173A>G (p.Gln58Arg)	TOR2A (Q58R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209955	NM_001085347.3(TOR2A):c.62T>C (p.Val21Ala)	LOC130002656, TOR2A (V21A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3245119	NC_000009.11:g.(?_130374683)_(131329276_?)del	AK1, BBLN +32 more	Deletion	Developmental and epileptic encephalopathy, 31A +1 more	GPathogenic
Select item 3245057	NC_000009.11:g.(?_130216807)_(133557056_?)dup	SH3GLB2, SLC25A25 +70 more	Duplication	Dystonic disorder	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 1711101	GRCh37/hg19 9p24.3-q34.11(chr9:203861-131603223)x3	ADAMTSL1, CEP78 +596 more	Copy number gain	See cases	GPathogenic
Select item 1527563	GRCh37/hg19 9q34.11(chr9:130392953-130526044)	CFAP157, PTRH1 +4 more	Copy number loss	not specified	GPathogenic
Select item 1527562	GRCh37/hg19 9q34.11(chr9:130390139-132760275)	AK1, ASB6 +62 more	Copy number loss	not specified	GPathogenic
Select item 1527561	GRCh37/hg19 9q34.11(chr9:130306022-130522616)	CFAP157, NIBAN2 +5 more	Copy number loss	not specified	GPathogenic
Select item 1527560	GRCh37/hg19 9q33.3-34.11(chr9:129079208-130851795)	AK1, ANGPTL2 +29 more	Copy number loss	not specified	GPathogenic
Select item 1527545	GRCh37/hg19 9q32-34.11(chr9:116422275-131713233)	ADGRD2, AK1 +141 more	Copy number gain	not specified	GPathogenic
Select item 1527491	GRCh37/hg19 9p24.3-q34.3(chr9:353349-141020389)	ANKRD18A, ANKRD18B +768 more	Copy number gain	not specified	GPathogenic
Select item 1457478	NC_000009.11:g.(?_130216807)_(130953136_?)del	AK1, BBLN +22 more	Deletion	Congenital muscular dystrophy with intellectual disability and severe epilepsy	GPathogenic
Select item 1340206	GRCh37/hg19 9q33.3-34.11(chr9:128523763-132604808)x3	AK1, ANGPTL2 +75 more	Copy number gain	not provided	GPathogenic
Select item 1056169	NC_000009.11:g.(?_129376729)_(131016993_?)del	ST6GALNAC6, AK1 +33 more	Deletion	Early infantile epileptic encephalopathy with suppression bursts	GPathogenic
Select item 984763	GRCh37/hg19 9q34.11(chr9:130412438-131423964)x1	COQ4, DNM1 +33 more	Copy number loss	Infantile epilepsy syndrome	GPathogenic
Select item 983307	GRCh37/hg19 9q33.3-34.11(chr9:128512347-130702572)x1	AK1, ANGPTL2 +27 more	Copy number loss	Developmental and epileptic encephalopathy, 4 +1 more	GPathogenic
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 685192	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020388)x3	MSMP, OR13D1 +769 more	Copy number gain	not provided	GPathogenic
Select item 625638	GRCh37/hg19 9q34.11(chr9:130335766-130517907)	CFAP157, NIBAN2 +5 more	Copy number loss	Developmental and epileptic encephalopathy, 4	GPathogenic
Select item 523294	GRCh37/hg19 9q21.11-34.3(chr9:71069743-140999928)	ISCA1, MIR32 +555 more	Copy number gain	Global developmental delay +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 395707	GRCh37/hg19 9p24.3-q34.3(chr9:62525-141006407)	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic
Select item 395356	GRCh37/hg19 9q33.3-34.3(chr9:128652785-141044751)x3	ABCA2, ABL1 +228 more	Copy number gain	See cases	GPathogenic
Select item 394948	GRCh37/hg19 9q33.2-34.3(chr9:124642754-141146461)x3	ABCA2, ABL1 +279 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

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Items: 74