Related gene-specific medical variations for Gene (Select 2877) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3102106	NM_002083.4(GPX2):c.91G>A (p.Val31Met)	CHURC1-FNTB, GPX2 (V31M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102105	NM_002083.4(GPX2):c.74C>T (p.Thr25Met)	CHURC1-FNTB, GPX2 (T25M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102104	NM_002083.4(GPX2):c.74C>A (p.Thr25Lys)	CHURC1-FNTB, GPX2 (T25K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102103	NM_002083.4(GPX2):c.512G>A (p.Arg171His)	CHURC1-FNTB, GPX2 (R171H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102102	NM_002083.4(GPX2):c.335A>T (p.Glu112Val)	CHURC1-FNTB, GPX2 (E112V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102101	NM_002083.4(GPX2):c.334G>A (p.Glu112Lys)	CHURC1-FNTB, GPX2 (E112K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3102100	NM_002083.4(GPX2):c.134G>A (p.Arg45Gln)	CHURC1-FNTB, GPX2 (R45Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2590738	NM_002083.4(GPX2):c.11T>C (p.Ile4Thr)	CHURC1-FNTB, GPX2 (I4T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2588207	NM_002083.4(GPX2):c.439C>T (p.Arg147Cys)	CHURC1-FNTB, GPX2 (R147C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2480988	NM_002083.4(GPX2):c.31C>T (p.Leu11Phe)	CHURC1-FNTB, GPX2 (L11F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2404725	NM_002083.4(GPX2):c.413A>G (p.Lys138Arg)	CHURC1-FNTB, GPX2 (K138R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2357728	NM_002083.4(GPX2):c.167G>A (p.Arg56His)	CHURC1-FNTB, GPX2 (R56H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2313080	NM_002083.4(GPX2):c.551G>T (p.Arg184Leu)	CHURC1-FNTB, GPX2 (R184L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance