"Ambry Genetics"[submitter] AND "GPX8"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282569	NM_001008397.4(GPX8):c.92C>T (p.Thr31Met)	CDC20B, GPX8 (T31M)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2252348	NM_001008397.4(GPX8):c.97T>C (p.Phe33Leu)	CDC20B, GPX8 (F33L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2469048	NM_001008397.4(GPX8):c.167A>G (p.Lys56Arg)	CDC20B, GPX8 (K56R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2281605	NM_001008397.4(GPX8):c.222C>G (p.Asn74Lys)	CDC20B, GPX8 (N23K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102124	NM_001008397.4(GPX8):c.269A>G (p.Lys90Arg)	CDC20B, GPX8 (K39R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2599146	NM_001008397.4(GPX8):c.365T>C (p.Val122Ala)	CDC20B, GPX8 (V122A +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2332710	NM_001008397.4(GPX8):c.371C>G (p.Ser124Cys)	CDC20B, GPX8 (S73C +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2235376	NM_001008397.4(GPX8):c.414C>G (p.His138Gln)	CDC20B, GPX8 (H87Q +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2515438	NM_001008397.4(GPX8):c.505T>G (p.Tyr169Asp)	CDC20B, GPX8 (Y76D +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3282568	NM_001008397.4(GPX8):c.605T>G (p.Ile202Ser)	CDC20B, GPX8 (I109S +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance