"Ambry Genetics"[submitter] AND "MDGA2"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3124585	NM_001113498.3(MDGA2):c.3056C>T (p.Ser1019Phe)	MDGA2 (S1019F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124584	NM_001113498.3(MDGA2):c.2609T>G (p.Ile870Ser)	MDGA2 (I572S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257954	NM_001113498.3(MDGA2):c.2519A>G (p.Gln840Arg)	MDGA2 (Q542R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3124583	NM_001113498.3(MDGA2):c.2203G>A (p.Asp735Asn)	MDGA2 (D735N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477270	NM_001113498.3(MDGA2):c.2167A>T (p.Ser723Cys)	MDGA2 (S723C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300392	NM_001113498.3(MDGA2):c.1876G>A (p.Val626Ile)	MDGA2 (V328I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482203	NM_001113498.3(MDGA2):c.1606G>A (p.Val536Ile)	MDGA2 (V238I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293810	NM_001113498.3(MDGA2):c.1346T>C (p.Leu449Ser)	MDGA2 (L151S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400163	NM_001113498.3(MDGA2):c.1246G>A (p.Asp416Asn)	MDGA2 (D118N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482701	NM_001113498.3(MDGA2):c.1168A>G (p.Lys390Glu)	MDGA2 (K390E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350974	NM_001113498.3(MDGA2):c.906T>G (p.Phe302Leu)	MDGA2 (F4L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282738	NM_001113498.3(MDGA2):c.886C>T (p.Pro296Ser)	MDGA2 (P296S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3293812	NM_001113498.3(MDGA2):c.777A>G (p.Glu259=)	MDGA2	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2271361	NM_001113498.3(MDGA2):c.686T>C (p.Val229Ala)	MDGA2 (V229A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3124586	NM_001113498.3(MDGA2):c.598T>A (p.Leu200Met)	MDGA2 (L200M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2487053	NM_001113498.3(MDGA2):c.568A>G (p.Ile190Val)	MDGA2 (I190V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2484580	NM_001113498.3(MDGA2):c.343T>G (p.Ser115Ala)	LOC126861933, MDGA2 (S115A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance