"Ambry Genetics"[submitter] AND "GLRX2"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2390748	NM_197962.3(GLRX2):c.485A>G (p.Glu162Gly)	GLRX2 (E162G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355328	NM_197962.3(GLRX2):c.451C>T (p.His151Tyr)	GLRX2 (H152Y +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2551991	NM_197962.3(GLRX2):c.299A>G (p.Asp100Gly)	GLRX2 (D101G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2256144	NM_197962.3(GLRX2):c.161C>A (p.Thr54Lys)	GLRX2 (T54K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2482177	NM_197962.3(GLRX2):c.157G>A (p.Ala53Thr)	GLRX2 (A13T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2532306	NM_197962.3(GLRX2):c.139T>C (p.Ser47Pro)	GLRX2 (S7P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2403354	NM_016066.4(GLRX2):c.77T>C (p.Ile26Thr)	GLRX2, LOC122149333 (I26T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2526069	NM_016066.4(GLRX2):c.10C>G (p.Arg4Gly)	GLRX2 (R4G)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GLikely benign