ClinVar for Gene (Select 10218) - ClinVar

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Links from Gene

Items: 77

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3247965	NC_000001.10:g.(?_5923325)_(12071622_?)del	KCNAB2, KIF1B +76 more	Deletion	not provided	GUncertain significance
Select item 3247909	NC_000001.10:g.(?_10710729)_(12030893_?)del	AGTRAP, ANGPTL7 +21 more	Deletion	not provided	GUncertain significance
Select item 3242274	GRCh37/hg19 1p36.32-36.12(chr1:4436802-22782007)x2	AADACL3, AADACL4 +207 more	Copy number loss	not provided	GPathogenic
Select item 3118896	NM_021146.4(ANGPTL7):c.925C>T (p.Arg309Cys)	ANGPTL7, MTOR (R309C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118891	NM_021146.4(ANGPTL7):c.911A>G (p.Asn304Ser)	ANGPTL7, MTOR (N304S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118885	NM_021146.4(ANGPTL7):c.863T>A (p.Leu288His)	ANGPTL7, LOC129388452 +1 more (L288H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118880	NM_021146.4(ANGPTL7):c.811T>A (p.Phe271Ile)	ANGPTL7, LOC129388452 +1 more (F271I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118877	NM_021146.4(ANGPTL7):c.691C>T (p.Arg231Cys)	ANGPTL7, LOC129388452 +1 more (R231C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118869	NM_021146.4(ANGPTL7):c.574A>C (p.Lys192Gln)	ANGPTL7, MTOR (K192Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118856	NM_021146.4(ANGPTL7):c.281G>A (p.Arg94Gln)	ANGPTL7, MTOR (R94Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118836	NM_021146.4(ANGPTL7):c.122A>G (p.Lys41Arg)	ANGPTL7, MTOR (K41R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3063399	GRCh37/hg19 1p36.31-36.21(chr1:6330828-12910774)x1	AADACL3, AADACL4 +80 more	Copy number loss	not specified	GPathogenic
Select item 3024678	NM_021146.4(ANGPTL7):c.658C>T (p.Arg220Cys)	ANGPTL7, MTOR (R220C)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2664871	GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3	LOC112577491, LOC112577504 +2149 more	Copy number gain	Trisomy 12p	GPathogenic
Select item 2638225	NM_021146.4(ANGPTL7):c.930G>A (p.Leu310=)	ANGPTL7, MTOR	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2638224	NM_021146.4(ANGPTL7):c.419G>A (p.Arg140His)	ANGPTL7, MTOR (R140H)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2621277	NM_021146.4(ANGPTL7):c.452A>C (p.Asp151Ala)	ANGPTL7, MTOR (D151A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600173	NM_021146.4(ANGPTL7):c.683G>C (p.Gly228Ala)	ANGPTL7, MTOR (G228A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2593124	NM_021146.4(ANGPTL7):c.1034A>G (p.Lys345Arg)	ANGPTL7, MTOR (K345R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591576	NM_021146.4(ANGPTL7):c.865C>T (p.Arg289Cys)	ANGPTL7, LOC129388452 +1 more (R289C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2557229	NM_021146.4(ANGPTL7):c.562T>C (p.Trp188Arg)	ANGPTL7, MTOR (W188R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533891	NM_021146.4(ANGPTL7):c.269G>A (p.Arg90His)	ANGPTL7, MTOR (R90H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531682	NM_021146.4(ANGPTL7):c.641G>T (p.Arg214Ile)	ANGPTL7, MTOR (R214I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2446820	NC_000001.10:g.4481271_20530242del	NOL9, TNFRSF1B +184 more	Deletion	Chromosome 1p36 deletion syndrome	GPathogenic
Select item 2426061	NC_000001.10:g.(?_9304994)_(12569078_?)dup	CENPS, CENPS-CORT +44 more	Duplication	Charcot-Marie-Tooth disease type 2	GUncertain significance
Select item 2425520	NC_000001.10:g.(?_10698999)_(11907741_?)dup	AGTRAP, ANGPTL7 +18 more	Duplication	Atrial fibrillation, familial, 6	GUncertain significance
Select item 2425278	NC_000001.10:g.(?_9770514)_(11264780_?)del	ANGPTL7, C1orf127 +20 more	Deletion	Immunodeficiency 14	GUncertain significance
Select item 2425245	NC_000001.10:g.(?_10753911)_(11854615_?)dup	AGTRAP, ANGPTL7 +16 more	Duplication	not provided	GUncertain significance
Select item 2340902	NM_021146.4(ANGPTL7):c.261C>G (p.Asn87Lys)	ANGPTL7, MTOR (N87K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337180	NM_021146.4(ANGPTL7):c.869A>G (p.Lys290Arg)	ANGPTL7, LOC129388452 +1 more (K290R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329899	NM_021146.4(ANGPTL7):c.1019G>A (p.Arg340His)	ANGPTL7, MTOR (R340H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302553	NM_021146.4(ANGPTL7):c.40A>G (p.Ile14Val)	ANGPTL7, MTOR (I14V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292064	NM_021146.4(ANGPTL7):c.268C>T (p.Arg90Cys)	ANGPTL7, MTOR (R90C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1808934	GRCh37/hg19 1p36.31-36.13(chr1:6758933-19287770)x1	AADACL3, AADACL4 +143 more	Copy number loss	not provided	GPathogenic
Select item 1808634	GRCh37/hg19 1p36.33-36.22(chr1:849467-12448956)x1	ACAP3, ACOT7 +159 more	Copy number loss	not provided	GPathogenic
Select item 1707471	NC_000001.11:g.10115497_16283149dup	LOC110120623, LOC110120648 +361 more	Duplication	not specified	GLikely pathogenic
Select item 1701093	NM_021146.4(ANGPTL7):c.525G>T (p.Gln175His)	ANGPTL7, MTOR (Q175H)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1340028	GRCh37/hg19 1p36.33-36.13(chr1:849466-17525065)x1	AJAP1, KAZN +228 more	Copy number loss	not provided	GPathogenic
Select item 980395	GRCh37/hg19 1p36.22(chr1:11192259-11432433)x3	ANGPTL7, UBIAD1 +1 more	Copy number gain	not provided	GUncertain significance
Select item 929342	GRCh37/hg19 1p36.22(chr1:11053101-11336968)x1	ANGPTL7, EXOSC10 +5 more	Copy number loss	See cases	GLikely pathogenic
Select item 830841	NC_000001.11:g.(?_11012634)_(11934865_?)del	DISP3, AGTRAP +19 more	Deletion	Atrial fibrillation, familial, 6	GUncertain significance
Select item 814055	GRCh37/hg19 1p36.22(chr1:11086990-11429365)x3	MTOR, UBIAD1 +4 more	Copy number gain	not provided	GUncertain significance
Select item 814053	GRCh37/hg19 1p36.22(chr1:9852396-11909475)x1	TARDBP, RBP7 +31 more	Copy number loss	not provided	GLikely pathogenic
Select item 685664	GRCh37/hg19 1p36.22-36.21(chr1:10246640-12841900)x1	AADACL3, AADACL4 +38 more	Copy number loss	not provided	GUncertain significance
Select item 638124	GRCh37/hg19 1p36.33-36.22(chr1:82154-11784118)x1	ACAP3, ACOT7 +148 more	Copy number loss	See cases	GPathogenic
Select item 635767	GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3	ANGPTL7, C1orf127 +783 more	Copy number gain	Intellectual disability, mild +1 more	GUncertain significance
Select item 443150	GRCh37/hg19 1p36.22-36.21(chr1:10722725-14267773)x1	AADACL3, AADACL4 +53 more	Copy number loss	See cases	GLikely pathogenic
Select item 442387	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	BCAS2, CNTN2 +2014 more	Copy number gain	See cases	GPathogenic
Select item 442386	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	FAM76A, FAM78B +2014 more	Copy number gain	See cases	GPathogenic
Select item 442266	GRCh37/hg19 1p36.22-36.21(chr1:11143298-13709344)x3	AADACL3, AADACL4 +43 more	Copy number gain	See cases	GUncertain significance
Select item 441991	GRCh37/hg19 1p36.22-36.21(chr1:10722955-12910774)x1	AADACL3, AADACL4 +34 more	Copy number loss	See cases	GLikely pathogenic
Select item 441913	GRCh37/hg19 1p36.23-36.13(chr1:8850514-16272383)x1	AADACL3, AADACL4 +97 more	Copy number loss	See cases	GLikely pathogenic
Select item 395144	GRCh37/hg19 1p36.32-36.21(chr1:4558588-13187457)x1	AADACL3, AADACL4 +96 more	Copy number loss	See cases	GPathogenic
Select item 253459	GRCh37/hg19 1p36.33-36.21(chr1:746608-15077159)x1	CCNL2, CDK11A +188 more	Copy number loss	See cases	GPathogenic
Select item 253358	GRCh37/hg19 1p36.23-36.21(chr1:8255222-12785220)x3	AGTRAP, DISP3 +56 more	Copy number gain	See cases	GLikely pathogenic
Select item 252976	GRCh37/hg19 1p36.33-36.22(chr1:82154-12699337)x1	ACAP3, ACOT7 +162 more	Copy number loss	See cases	GPathogenic
Select item 221357	chr1:909238-16736132 complex variant	RER1, RERE +212 more	Complex	Breast ductal adenocarcinoma	GUncertain significance
Select item 221334	Single allele	IGSF21, IL22RA1 +314 more	Complex	Breast ductal adenocarcinoma	GUncertain significance
Select item 154839	GRCh38/hg38 1p36.31-36.13(chr1:6554885-16056011)x3	AADACL3, AADACL4 +563 more	Copy number gain	See cases	GPathogenic
Select item 154704	GRCh38/hg38 1p36.31-36.13(chr1:5363826-18360302)x1	PLOD1, PRAMEF1 +730 more	Copy number loss	See cases	GPathogenic
Select item 153434	GRCh38/hg38 1p36.22-36.21(chr1:11021751-15236671)x3	AADACL3, AADACL4 +209 more	Copy number gain	See cases	GLikely pathogenic
Select item 152937	GRCh38/hg38 1p36.22-36.21(chr1:10264397-15780840)x1	AADACL3, AADACL4 +304 more	Copy number loss	See cases	GPathogenic
Select item 152293	GRCh38/hg38 1p36.22-36.21(chr1:9428538-15815791)x1	AADACL3, AADACL4 +370 more	Copy number loss	See cases	GPathogenic
Select item 148885	GRCh38/hg38 1p36.31-36.21(chr1:6303641-15799093)x1	LOC129929327, LOC129929328 +557 more	Copy number loss	See cases	GPathogenic
Select item 148387	GRCh38/hg38 1p36.32-36.21(chr1:4898439-12911913)x1	AADACL3, AADACL4 +500 more	Copy number loss	See cases	GPathogenic
Select item 147521	GRCh38/hg38 1p36.33-36.22(chr1:844347-12470133)x1	ACAP3, ACOT7 +806 more	Copy number loss	See cases	GPathogenic
Select item 146535	GRCh38/hg38 1p36.23-36.22(chr1:8283694-12470133)x1	AGTRAP, ANGPTL7 +309 more	Copy number loss	See cases	GPathogenic
Select item 144297	GRCh38/hg38 1p36.23-36.21(chr1:9064492-12666744)x1	AADACL4, AGTRAP +280 more	Copy number loss	See cases	GPathogenic
Select item 59895	GRCh38/hg38 1p36.22-36.13(chr1:11121625-16324498)x1	AADACL3, AADACL4 +288 more	Copy number loss	See cases	GPathogenic
Select item 59894	GRCh38/hg38 1p36.22-36.13(chr1:10809039-16422500)x1	LOC112577504, LOC112577505 +316 more	Copy number loss	See cases	GPathogenic
Select item 59892	GRCh38/hg38 1p36.22-36.13(chr1:10621776-16520709)x1	AADACL3, AADACL4 +337 more	Copy number loss	See cases	GPathogenic
Select item 59885	GRCh38/hg38 1p36.23-36.13(chr1:9034671-16441465)x1	AADACL3, AADACL4 +462 more	Copy number loss	See cases	GPathogenic
Select item 59884	GRCh38/hg38 1p36.23-36.21(chr1:7165036-13111056)x1	AADACL3, AADACL4 +386 more	Copy number loss	See cases	GPathogenic
Select item 59856	GRCh38/hg38 1p36.32-36.21(chr1:4898439-13111056)x1	LOC129929435, LOC129929436 +505 more	Copy number loss	See cases	GPathogenic
Select item 59846	GRCh38/hg38 1p36.32-36.13(chr1:3006193-17688934)x1	LINC02783, LINC03126 +804 more	Copy number loss	See cases	GPathogenic
Select item 58051	GRCh38/hg38 1p36.31-36.21(chr1:6652339-12724844)x3	AADACL3, AADACL4 +387 more	Copy number gain	See cases	GPathogenic
Select item 57720	GRCh38/hg38 1p36.22(chr1:10637036-11293430)x3	ANGPTL7, C1orf127 +43 more	Copy number gain	See cases	GUncertain significance

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Links from Gene

Items: 77