"PreventionGenetics, part of Exact Sciences"[submitter] AND "AGO1"[gen - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 744858	NM_012199.5(AGO1):c.33C>T (p.Gly11=)	AGO1	Single nucleotide variant (synonymous variant +1 more)	AGO1-related disorder +1 more	GLikely benign
Select item 2631332	NM_012199.5(AGO1):c.77G>A (p.Arg26Gln)	AGO1 (R26Q)	Single nucleotide variant (missense variant +1 more)	AGO1-related disorder	GUncertain significance
Select item 787855	NM_012199.5(AGO1):c.165C>T (p.Tyr55=)	AGO1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 3053726	NM_012199.5(AGO1):c.465G>A (p.Glu155=)	AGO1	Single nucleotide variant (synonymous variant)	AGO1-related disorder	GLikely benign
Select item 2630643	NM_012199.5(AGO1):c.496C>T (p.His166Tyr)	AGO1 (H166Y +1 more)	Single nucleotide variant (missense variant)	AGO1-related disorder	GUncertain significance
Select item 3060004	NM_012199.5(AGO1):c.681A>G (p.Pro227=)	AGO1	Single nucleotide variant (synonymous variant)	AGO1-related disorder	GBenign
Select item 1251924	NM_012199.5(AGO1):c.1123GAG[1] (p.Glu376del)	AGO1 (E301del +1 more)	Microsatellite (inframe_deletion)	not specified +2 more	GPathogenic/Likely pathogenic
Select item 2635260	NM_012199.5(AGO1):c.2246G>A (p.Cys749Tyr)	AGO1 (C674Y +1 more)	Single nucleotide variant (missense variant)	AGO1-related disorder	GUncertain significance
Select item 3038075	NM_012199.5(AGO1):c.2265+4G>T	AGO1	Single nucleotide variant (intron variant)	AGO1-related disorder	GBenign