ClinVar for Gene (Select 56986) - ClinVar

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Links from Gene

Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3273960	NM_001144955.2(DTWD1):c.581G>T (p.Cys194Phe)	DTWD1 (C194F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273959	NM_001144955.2(DTWD1):c.286A>G (p.Ile96Val)	DTWD1 (I96V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273958	NM_001144955.2(DTWD1):c.823G>A (p.Asp275Asn)	DTWD1 (D275N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3273957	NM_001144955.2(DTWD1):c.713G>A (p.Arg238His)	DTWD1 (R238H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086093	NM_001144955.2(DTWD1):c.701C>T (p.Thr234Ile)	DTWD1 (T234I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086092	NM_001144955.2(DTWD1):c.311G>A (p.Gly104Asp)	DTWD1 (G104D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086091	NM_001144955.2(DTWD1):c.119G>A (p.Cys40Tyr)	DTWD1, LOC126862129 (C40Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063396	GRCh37/hg19 15q21.1-21.2(chr15:49143050-50410530)x1	ATP8B4, COPS2 +7 more	Copy number loss	not specified	GUncertain significance
Select item 3063379	GRCh37/hg19 15q11.2-21.2(chr15:22770421-50347130)x3	ACTC1, ADAL +200 more	Copy number gain	not specified	GPathogenic
Select item 2685513	GRCh37/hg19 15q21.1-21.3(chr15:49390592-56800964)x1	TMOD2, USP50 +43 more	Copy number loss	not provided	GPathogenic
Select item 2671612	Single allele	ADAL, AFG2B +103 more	Deletion	not provided	GPathogenic
Select item 2578751	GRCh37/hg19 15q21.2(chr15:49775348-51221365)x1	AP4E1, ATP8B4 +10 more	Copy number loss	not provided	GUncertain significance
Select item 2559073	NM_001144955.2(DTWD1):c.496G>A (p.Gly166Ser)	DTWD1 (G166S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531575	NM_001144955.2(DTWD1):c.613A>G (p.Ile205Val)	DTWD1 (I205V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469729	NM_001144955.2(DTWD1):c.254C>T (p.Pro85Leu)	DTWD1, LOC126862129 (P85L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317879	NM_001144955.2(DTWD1):c.184G>A (p.Gly62Ser)	DTWD1, LOC126862129 (G62S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225215	NM_001144955.2(DTWD1):c.182G>A (p.Cys61Tyr)	DTWD1, LOC126862129 (C61Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1807706	GRCh37/hg19 15q21.1-22.2(chr15:48589845-63543438)x3	ADAM10, ALDH1A2 +81 more	Copy number gain	not provided	GPathogenic
Select item 1526455	GRCh37/hg19 15q21.1-21.2(chr15:48940736-51309941)	AP4E1, ATP8B4 +16 more	Copy number loss	not specified	GUncertain significance
Select item 1526453	GRCh37/hg19 15q21.1-21.3(chr15:47635238-56509908)	CEP152, COPS2 +52 more	Copy number loss	not specified	GPathogenic
Select item 1526451	GRCh37/hg19 15q21.1-21.2(chr15:47574384-50369056)	EID1, FAM227B +15 more	Copy number loss	not specified	GPathogenic
Select item 1024934	NC_000015.9:g.(?_32964879)_(91358519_?)dup	CGNL1, MAPDA +472 more	Duplication	Familial colorectal cancer +1 more	GUncertain significance
Select item 988929	GRCh37/hg19 15q21.1-21.3(chr15:48744917-53851050)x1	AP4E1, ARPP19 +35 more	Copy number loss	not provided	GPathogenic
Select item 815710	GRCh37/hg19 15q21.1-21.2(chr15:47192561-50819726)x1	ATP8B4, CEP152 +20 more	Copy number loss	not provided	GPathogenic
Select item 688584	GRCh37/hg19 15q21.1-21.3(chr15:49031132-56740397)x3	AP4E1, ARPP19 +47 more	Copy number gain	not provided	GPathogenic
Select item 685183	GRCh37/hg19 15q21.1-22.2(chr15:48000433-60747551)x3	ADAM10, ALDH1A2 +76 more	Copy number gain	not provided	GPathogenic
Select item 564197	GRCh37/hg19 15q15.3-21.3(chr15:43759773-53252240)x1	AP4E1, ARPP19 +76 more	Copy number loss	not provided	GPathogenic
Select item 560049	Single allele	PDIA3, PEAK1 +521 more	Duplication	not provided	GPathogenic
Select item 443456	GRCh37/hg19 15q21.2(chr15:49656531-50165554)x3	ATP8B4, DTWD1 +2 more	Copy number gain	See cases	GLikely benign
Select item 442893	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3	AAGAB, ABHD17C +559 more	Copy number gain	See cases	GPathogenic
Select item 442892	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)	NOX5, NPAP1 +559 more	Copy number gain	See cases	GPathogenic
Select item 395389	GRCh37/hg19 15q15.1-21.2(chr15:41689327-52446981)x1	ADAL, AFG2B +107 more	Copy number loss	See cases	GPathogenic
Select item 395145	GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4	CHRFAM7A, CHRM5 +566 more	Copy number gain	See cases	GPathogenic
Select item 394887	GRCh37/hg19 15q15.1-26.3(chr15:41745084-102354798)x4	ALDH1A2, ALDH1A3 +444 more	Copy number gain	See cases	GPathogenic
Select item 148540	GRCh38/hg38 15q21.1-21.2(chr15:49064333-50176783)x1	ATP8B4, COPS2 +18 more	Copy number loss	See cases	GUncertain significance
Select item 146334	GRCh38/hg38 15q21.1-21.2(chr15:47460844-52494222)x1	AP4E1, ATP8B4 +190 more	Copy number loss	See cases	GPathogenic

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Links from Gene

Items: 36