"ARID5B-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3042690	NM_032199.3(ARID5B):c.22-6dup	ARID5B	Duplication (intron variant)	ARID5B-related condition	GLikely benign
Select item 2635514	NM_032199.3(ARID5B):c.137G>A (p.Cys46Tyr)	ARID5B (C46Y)	Single nucleotide variant (missense variant)	ARID5B-related condition	GUncertain significance
Select item 3048787	NM_032199.3(ARID5B):c.375C>T (p.His125=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 3040475	NM_032199.3(ARID5B):c.628C>T (p.Leu210=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 3055153	NM_032199.3(ARID5B):c.771A>G (p.Pro257=)	ARID5B, LOC126860943	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 3054545	NM_032199.3(ARID5B):c.1497G>A (p.Gly499=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 3042667	NM_032199.3(ARID5B):c.1599G>A (p.Ala533=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 3037676	NM_032199.3(ARID5B):c.1812G>A (p.Pro604=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GBenign
Select item 3040724	NM_032199.3(ARID5B):c.1852G>A (p.Ala618Thr)	ARID5B (A375T +1 more)	Single nucleotide variant (missense variant)	ARID5B-related condition	GBenign
Select item 3038643	NM_032199.3(ARID5B):c.1908C>T (p.Asp636=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 3035588	NM_032199.3(ARID5B):c.2235G>A (p.Ala745=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 3044584	NM_032199.3(ARID5B):c.2402T>C (p.Val801Ala)	ARID5B (V558A +1 more)	Single nucleotide variant (missense variant)	ARID5B-related condition	GBenign
Select item 3031682	NM_032199.3(ARID5B):c.2448A>G (p.Lys816=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 3036405	NM_032199.3(ARID5B):c.2562C>A (p.Ser854=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 3055195	NM_032199.3(ARID5B):c.2655G>A (p.Thr885=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 783575	NM_032199.3(ARID5B):c.2913G>A (p.Ser971=)	ARID5B	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3031676	NM_032199.3(ARID5B):c.3084C>T (p.Ala1028=)	ARID5B	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign