"Ambry Genetics"[submitter] AND "MTX3"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2239896	NM_001363818.2(MTX3):c.809A>G (p.Glu270Gly)	MTX3 (E270G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288879	NM_001363818.2(MTX3):c.766G>A (p.Val256Ile)	MTX3 (V195I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354808	NM_001363818.2(MTX3):c.755G>A (p.Gly252Glu)	MTX3 (G191E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3218798	NM_001363818.2(MTX3):c.734T>C (p.Leu245Pro)	MTX3 (L184P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296819	NM_001363818.2(MTX3):c.731G>A (p.Ser244Asn)	MTX3 (S183N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218795	NM_001363818.2(MTX3):c.592T>G (p.Leu198Val)	MTX3 (L137V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218792	NM_001363818.2(MTX3):c.583C>T (p.Pro195Ser)	MTX3 (P134S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210576	NM_001363818.2(MTX3):c.578A>C (p.Asp193Ala)	MTX3 (D132A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296820	NM_001363818.2(MTX3):c.547A>G (p.Arg183Gly)	MTX3 (R122G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274456	NM_001363818.2(MTX3):c.515A>T (p.Asp172Val)	MTX3 (D111V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243870	NM_001363818.2(MTX3):c.493G>A (p.Val165Met)	MTX3 (V165M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331853	NM_001363818.2(MTX3):c.481C>T (p.His161Tyr)	MTX3 (H100Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237703	NM_001363818.2(MTX3):c.406T>G (p.Leu136Val)	MTX3 (L75V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296818	NM_001363818.2(MTX3):c.375G>T (p.Trp125Cys)	MTX3 (W125C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550195	NM_001363818.2(MTX3):c.307C>T (p.Leu103Phe)	MTX3 (L103F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390307	NM_001363818.2(MTX3):c.257C>G (p.Ala86Gly)	MTX3 (A86G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218808	NM_001363818.2(MTX3):c.256G>A (p.Ala86Thr)	MTX3 (A25T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218804	NM_001363818.2(MTX3):c.238G>A (p.Ala80Thr)	MTX3 (A19T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance