Related gene-specific medical variations for Gene (Select 441376) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3261424	NM_001025357.3(AARD):c.245C>T (p.Ala82Val)	AARD, LOC130000997 (A82V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134916	NM_001025357.3(AARD):c.299C>T (p.Thr100Ile)	AARD, LOC130000997 (T100I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134892	NM_001025357.3(AARD):c.274C>G (p.Gln92Glu)	AARD, LOC130000997 (Q92E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3134862	NM_001025357.3(AARD):c.254C>G (p.Ala85Gly)	AARD, LOC130000997 (A85G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2681196	NM_001025357.3(AARD):c.244GCG[8] (p.Ala88_Arg89insAla)	AARD, LOC130000997	Microsatellite (inframe_insertion)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign

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