"Ambry Genetics"[submitter] AND "AGO3"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2307840	NM_024852.4(AGO3):c.36G>C (p.Gln12His)	AGO3 (Q12H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361230	NM_024852.4(AGO3):c.287A>G (p.Asn96Ser)	AGO3 (N96S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238683	NM_024852.4(AGO3):c.298G>A (p.Val100Met)	AGO3 (V100M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096271	NM_024852.4(AGO3):c.391G>T (p.Val131Leu)	AGO3 (V131L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2260400	NM_024852.4(AGO3):c.439G>A (p.Glu147Lys)	AGO3 (E147K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241746	NM_024852.4(AGO3):c.622C>T (p.Arg208Trp)	AGO3 (R208W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2261104	NM_024852.4(AGO3):c.1171A>G (p.Thr391Ala)	AGO3 (T157A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551629	NM_024852.4(AGO3):c.1187A>G (p.Gln396Arg)	AGO3 (Q162R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553330	NM_024852.4(AGO3):c.1357G>T (p.Ala453Ser)	AGO3 (A219S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096250	NM_024852.4(AGO3):c.1399A>G (p.Ile467Val)	AGO3 (I233V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554369	NM_024852.4(AGO3):c.1427G>A (p.Arg476His)	AGO3 (R476H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2566102	NM_024852.4(AGO3):c.1738G>C (p.Val580Leu)	AGO3, LOC126805696 (V580L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096259	NM_024852.4(AGO3):c.2140A>T (p.Thr714Ser)	AGO3 (T480S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617658	NM_024852.4(AGO3):c.2321G>C (p.Cys774Ser)	AGO3 (C774S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276186	NM_024852.4(AGO3):c.2468A>G (p.His823Arg)	AGO3 (H589R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance