"Ambry Genetics"[submitter] AND "GPX5"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3102113	NM_001509.3(GPX5):c.18G>C (p.Arg6Ser)	GPX5 (R6S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303836	NM_001509.3(GPX5):c.94T>G (p.Cys32Gly)	GPX5 (C32G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456615	NM_001509.3(GPX5):c.208G>A (p.Ala70Thr)	GPX5 (A70T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2488404	NM_001509.3(GPX5):c.217T>C (p.Cys73Arg)	GPX5 (C73R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102114	NM_001509.3(GPX5):c.220G>T (p.Gly74Cys)	GPX5 (G74C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623648	NM_001509.3(GPX5):c.236A>C (p.Tyr79Ser)	GPX5 (Y79S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102115	NM_001509.3(GPX5):c.274T>G (p.Tyr92Asp)	GPX5 (Y92D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211635	NM_001509.3(GPX5):c.275A>G (p.Tyr92Cys)	GPX5 (Y92C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282565	NM_001509.3(GPX5):c.301T>G (p.Cys101Gly)	GPX5 (C101G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2219094	NM_001509.3(GPX5):c.344T>A (p.Ile115Asn)	GPX5 (I115N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288581	NM_001509.3(GPX5):c.367C>T (p.Arg123Cys)	GPX5 (R123C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102116	NM_001509.3(GPX5):c.445T>C (p.Phe149Leu)	GPX5 (F149L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102117	NM_001509.3(GPX5):c.466T>C (p.Cys156Arg)	GPX5 (C156R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2490862	NM_001509.3(GPX5):c.481G>A (p.Glu161Lys)	GPX5 (E161K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102118	NM_001509.3(GPX5):c.601C>T (p.Arg201Trp)	GPX5 (R201W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102119	NM_001509.3(GPX5):c.638C>A (p.Ala213Glu)	GPX5 (A213E)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign