ClinVar for Gene (Select 379) - ClinVar

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Links from Gene

Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3315143	NM_001661.4(ARL4D):c.251G>C (p.Arg84Pro)	ARL4D (R84P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315132	NM_001661.4(ARL4D):c.92C>T (p.Ser31Phe)	ARL4D (S31F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3243158	NC_000017.10:g.(?_41277268)_(41836109_?)dup	ARL4D, BRCA1 +7 more	Duplication	not provided	GUncertain significance
Select item 3129559	NM_001661.4(ARL4D):c.37T>G (p.Ser13Ala)	ARL4D (S13A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3129558	NM_001661.4(ARL4D):c.337A>G (p.Lys113Glu)	ARL4D (K113E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129557	NM_001661.4(ARL4D):c.26C>T (p.Ala9Val)	ARL4D (A9V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2681403	NM_001661.4(ARL4D):c.350A>G (p.His117Arg)	ARL4D (H117R)	Single nucleotide variant (missense variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2607206	NM_001661.4(ARL4D):c.286G>A (p.Gly96Ser)	ARL4D (G96S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556224	NM_001661.4(ARL4D):c.464G>C (p.Arg155Pro)	ARL4D (R155P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468936	NM_001661.4(ARL4D):c.138T>G (p.Phe46Leu)	ARL4D (F46L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262540	NM_001661.4(ARL4D):c.142C>G (p.Gln48Glu)	ARL4D (Q48E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1526577	GRCh37/hg19 17q21.31(chr17:41202796-41974964)	ARL4D, BRCA1 +12 more	Copy number gain	not specified	GUncertain significance
Select item 980720	GRCh37/hg19 17q21.31(chr17:41221565-41775043)x3	ARL4D, BRCA1 +6 more	Copy number gain	not provided	GUncertain significance
Select item 815937	GRCh37/hg19 17q21.31(chr17:41399892-42125780)x3	ARL4D, CD300LG +13 more	Copy number gain	not provided	GUncertain significance
Select item 815936	GRCh37/hg19 17q21.31(chr17:41399892-41736186)x3	ARL4D, DHX8 +2 more	Copy number gain	not provided	GUncertain significance
Select item 815935	GRCh37/hg19 17q21.31(chr17:41384515-41599383)x4	ARL4D, DHX8	Copy number gain	not provided	GUncertain significance
Select item 685524	GRCh37/hg19 17q21.31(chr17:41440122-41745139)x3	ARL4D, DHX8 +2 more	Copy number gain	not provided	GUncertain significance
Select item 584346	NC_000017.10:g.(?_41276016)_(41635727_?)dup	ARL4D, BRCA1 +5 more	Duplication	Hereditary breast ovarian cancer syndrome	GUncertain significance
Select item 547109	GRCh37/hg19 17q21.31(chr17:41464491-41835873)x3	ARL4D, DHX8 +3 more	Copy number gain	not provided	GLikely benign
Select item 442490	GRCh37/hg19 17q21.31(chr17:41213892-41554856)x3	ARL4D, BRCA1 +3 more	Copy number gain	See cases	GUncertain significance
Select item 441816	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	ALOX12, ALOX12B +1143 more	Copy number gain	See cases	GPathogenic
Select item 441815	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	SPEM2, TBCD +1143 more	Copy number gain	See cases	GPathogenic
Select item 155568	GRCh38/hg38 17q21.31(chr17:43050945-43897883)x3	ARL4D, BRCA1 +52 more	Copy number gain	See cases	GUncertain significance
Select item 154024	GRCh38/hg38 17q21.31(chr17:43322528-43849385)x3	ARL4D, CD300LG +33 more	Copy number gain	See cases	GLikely benign
Select item 150635	GRCh38/hg38 17q21.31(chr17:43124234-43520458)x3	ARL4D, BRCA1 +24 more	Copy number gain	See cases	GUncertain significance
Select item 150167	GRCh38/hg38 17q21.31(chr17:43088882-43865172)x3	ARL4D, BRCA1 +50 more	Copy number gain	See cases	GUncertain significance
Select item 148621	GRCh38/hg38 17q21.31(chr17:43080123-43897875)x3	ARL4D, BRCA1 +52 more	Copy number gain	See cases	GUncertain significance
Select item 148363	GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3	AARSD1, AATF +2032 more	Copy number gain	See cases	GPathogenic
Select item 148000	GRCh38/hg38 17q21.31(chr17:43387123-43865083)x3	ARL4D, CD300LG +26 more	Copy number gain	See cases	GUncertain significance
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	LOC130060786, LOC130060787 +633 more	Copy number gain	See cases	GPathogenic
Select item 57282	GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3	LOC126862582, LOC126862583 +1753 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 31