Related gene-specific medical variations for Gene (Select 92312) - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294478	NM_001093725.2(MEX3A):c.1019G>A (p.Gly340Asp)	LOC122128444, MEX3A (G340D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125623	NM_001093725.2(MEX3A):c.980G>T (p.Gly327Val)	LOC122128444, MEX3A (G327V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125621	NM_001093725.2(MEX3A):c.938T>A (p.Ile313Asn)	LOC122128444, MEX3A (I313N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125620	NM_001093725.2(MEX3A):c.836G>A (p.Arg279His)	LOC122128444, MEX3A (R279H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125617	NM_001093725.2(MEX3A):c.1375G>C (p.Gly459Arg)	LOC122128444, MEX3A (G459R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612390	NM_001093725.2(MEX3A):c.979G>A (p.Gly327Ser)	LOC122128444, MEX3A (G327S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557767	NM_001093725.2(MEX3A):c.646G>A (p.Val216Met)	LOC122128444, MEX3A (V216M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512666	NM_001093725.2(MEX3A):c.1264C>A (p.Pro422Thr)	LOC122128444, MEX3A (P422T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492133	NM_001093725.2(MEX3A):c.970C>T (p.His324Tyr)	LOC122128444, MEX3A (H324Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475935	NM_001093725.2(MEX3A):c.1502C>G (p.Thr501Arg)	LOC122128444, MEX3A (T501R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371934	NM_001093725.2(MEX3A):c.1184A>T (p.Gln395Leu)	LOC122128444, MEX3A (Q395L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358314	NM_001093725.2(MEX3A):c.1225T>G (p.Ser409Ala)	LOC122128444, MEX3A (S409A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320717	NM_001093725.2(MEX3A):c.1424G>A (p.Ser475Asn)	LOC122128444, MEX3A (S475N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273148	NM_001093725.2(MEX3A):c.923G>A (p.Ser308Asn)	LOC122128444, MEX3A (S308N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260467	NM_001093725.2(MEX3A):c.1027G>A (p.Gly343Ser)	LOC122128444, MEX3A (G343S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242514	NM_001093725.2(MEX3A):c.1379T>A (p.Leu460Gln)	LOC122128444, MEX3A (L460Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance