Related gene-specific medical variations for Gene (Select 10335) - ClinVar - NCBI

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Links from Gene

Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3286476	NM_130385.4(IRAG1):c.2539A>C (p.Lys847Gln)	IRAG1, IRAG1-AS1 (K532Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110750	NM_130385.4(IRAG1):c.2624A>T (p.Tyr875Phe)	IRAG1, IRAG1-AS1 (Y669F +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110748	NM_130385.4(IRAG1):c.2372G>A (p.Gly791Asp)	IRAG1, IRAG1-AS1 (G476D +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110747	NM_130385.4(IRAG1):c.2317C>A (p.Gln773Lys)	IRAG1, IRAG1-AS1 (Q753K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110745	NM_130385.4(IRAG1):c.2192G>A (p.Gly731Glu)	IRAG1, IRAG1-AS1 (G416E +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110744	NM_130385.4(IRAG1):c.2177C>T (p.Ser726Leu)	IRAG1, IRAG1-AS1 (S411L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110743	NM_130385.4(IRAG1):c.2074C>T (p.Pro692Ser)	IRAG1, IRAG1-AS1 (P601S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3110742	NM_130385.4(IRAG1):c.2033G>T (p.Arg678Leu)	IRAG1, IRAG1-AS1 +1 more (R587L +5 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3110741	NM_130385.4(IRAG1):c.2033G>A (p.Arg678His)	IRAG1, IRAG1-AS1 +1 more (R587H +5 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2614977	NM_130385.4(IRAG1):c.2600T>C (p.Val867Ala)	IRAG1, IRAG1-AS1 (V847A +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540570	NM_130385.4(IRAG1):c.2429G>A (p.Ser810Asn)	IRAG1, IRAG1-AS1 (S802N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536070	NM_130385.4(IRAG1):c.2545T>C (p.Cys849Arg)	IRAG1, IRAG1-AS1 (C758R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance