ClinVar for Gene (Select 138199) - ClinVar

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Links from Gene

Items: 65

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3263329	NM_152420.3(CARNMT1):c.748A>C (p.Lys250Gln)	CARNMT1 (K171Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263328	NM_152420.3(CARNMT1):c.62G>C (p.Gly21Ala)	CARNMT1, LOC130001900 (G21A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263327	NM_152420.3(CARNMT1):c.1058A>G (p.Asn353Ser)	CARNMT1, CARNMT1-AS1 (N274S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263326	NM_152420.3(CARNMT1):c.79G>A (p.Glu27Lys)	CARNMT1, LOC130001900 (E27K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137394	NM_152420.3(CARNMT1):c.88G>A (p.Val30Met)	CARNMT1, LOC130001900 (V30M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137393	NM_152420.3(CARNMT1):c.857G>T (p.Gly286Val)	CARNMT1 (G207V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137392	NM_152420.3(CARNMT1):c.76G>A (p.Glu26Lys)	CARNMT1, LOC130001900 (E26K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137391	NM_152420.3(CARNMT1):c.742A>G (p.Ile248Val)	CARNMT1 (I248V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137390	NM_152420.3(CARNMT1):c.584A>G (p.Glu195Gly)	CARNMT1 (E116G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137389	NM_152420.3(CARNMT1):c.364A>G (p.Ile122Val)	CARNMT1 (I43V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137388	NM_152420.3(CARNMT1):c.188G>A (p.Arg63His)	CARNMT1, LOC130001900 (R63H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137387	NM_152420.3(CARNMT1):c.184G>C (p.Glu62Gln)	CARNMT1, LOC130001900 (E62Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3063084	GRCh37/hg19 9q21.13(chr9:76897502-78586137)x3	C9orf40, CARNMT1 +6 more	Copy number gain	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 2616345	NM_152420.3(CARNMT1):c.248G>A (p.Arg83Gln)	CARNMT1 (R4Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606321	NM_152420.3(CARNMT1):c.65G>A (p.Gly22Asp)	CARNMT1, LOC130001900 (G22D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559880	NM_152420.3(CARNMT1):c.1154C>T (p.Thr385Ile)	CARNMT1, CARNMT1-AS1 (T385I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534158	NM_152420.3(CARNMT1):c.1122G>C (p.Lys374Asn)	CARNMT1, CARNMT1-AS1 (K295N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532281	NM_152420.3(CARNMT1):c.583G>C (p.Glu195Gln)	CARNMT1 (E195Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508222	NM_152420.3(CARNMT1):c.324C>A (p.His108Gln)	CARNMT1 (H29Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410098	NM_152420.3(CARNMT1):c.186G>T (p.Glu62Asp)	CARNMT1, LOC130001900 (E62D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340258	NM_152420.3(CARNMT1):c.1060G>A (p.Glu354Lys)	CARNMT1, CARNMT1-AS1 (E354K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289579	NM_152420.3(CARNMT1):c.366A>G (p.Ile122Met)	CARNMT1 (I122M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2245298	NM_152420.3(CARNMT1):c.322C>T (p.His108Tyr)	CARNMT1 (H29Y +1 more)	Single nucleotide variant (missense variant +1 more)	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 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 996578	NM_152420.3(CARNMT1):c.230G>A (p.Gly77Asp)	CARNMT1, LOC130001900 (G77D)	Single nucleotide variant (missense variant +1 more)	Intellectual disability	GLikely pathogenic
Select item 782145	NM_152420.3(CARNMT1):c.885T>C (p.Asp295=)	CARNMT1	Single nucleotide variant (synonymous variant +1 more)	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 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 563664	GRCh37/hg19 9q21.13(chr9:77449280-78560923)x1	PCSK5, CARNMT1 +5 more	Copy number loss	not provided	GUncertain significance
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 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 154945	GRCh38/hg38 9p24.3-q21.31(chr9:193412-79877816)x3	CDKN2B, CDKN2B-AS1 +1214 more	Copy number gain	See cases	GPathogenic
Select item 153582	GRCh38/hg38 9q21.13(chr9:74282586-75968293)x3	C9orf40, CARNMT1 +24 more	Copy number gain	See cases	GUncertain significance
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 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 144150	GRCh38/hg38 9q21.11-21.13(chr9:68454847-76252863)x1	ABHD17B, ALDH1A1 +148 more	Copy number loss	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 59087	GRCh38/hg38 9q21.13(chr9:74887986-75718195)x1	C9orf40, CARNMT1 +11 more	Copy number loss	See cases	GUncertain significance
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: 65