"Ambry Genetics"[submitter] AND "NTN3"[gene] - ClinVar

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Items: 47

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3202595	NM_006181.3(NTN3):c.82G>A (p.Asp28Asn)	NTN3 (D28N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301286	NM_006181.3(NTN3):c.104G>C (p.Gly35Ala)	NTN3 (G35A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346328	NM_006181.3(NTN3):c.106G>A (p.Ala36Thr)	NTN3 (A36T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202589	NM_006181.3(NTN3):c.112C>G (p.Arg38Gly)	NTN3 (R38G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331100	NM_006181.3(NTN3):c.138C>G (p.Asn46Lys)	NTN3 (N46K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383056	NM_006181.3(NTN3):c.205G>A (p.Ala69Thr)	NTN3 (A69T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202591	NM_006181.3(NTN3):c.221G>C (p.Arg74Pro)	NTN3 (R74P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474811	NM_006181.3(NTN3):c.248C>T (p.Ser83Phe)	NTN3 (S83F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351192	NM_006181.3(NTN3):c.257G>A (p.Gly86Asp)	NTN3 (G86D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344875	NM_006181.3(NTN3):c.260C>T (p.Thr87Met)	NTN3 (T87M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336021	NM_006181.3(NTN3):c.290C>A (p.Ser97Tyr)	NTN3 (S97Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202592	NM_006181.3(NTN3):c.352G>T (p.Val118Phe)	NTN3 (V118F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569819	NM_006181.3(NTN3):c.418C>T (p.His140Tyr)	NTN3 (H140Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202593	NM_006181.3(NTN3):c.419A>G (p.His140Arg)	NTN3 (H140R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279897	NM_006181.3(NTN3):c.424C>G (p.Arg142Gly)	NTN3 (R142G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369379	NM_006181.3(NTN3):c.512C>T (p.Pro171Leu)	NTN3 (P171L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231367	NM_006181.3(NTN3):c.545T>C (p.Leu182Pro)	NTN3 (L182P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202594	NM_006181.3(NTN3):c.625C>T (p.Pro209Ser)	NTN3 (P209S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623722	NM_006181.3(NTN3):c.703G>A (p.Asp235Asn)	NTN3 (D235N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465292	NM_006181.3(NTN3):c.761G>A (p.Arg254His)	NTN3 (R254H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274047	NM_006181.3(NTN3):c.763T>A (p.Cys255Ser)	NTN3 (C255S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202596	NM_006181.3(NTN3):c.869C>A (p.Pro290His)	NTN3 (P290H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467605	NM_006181.3(NTN3):c.880G>A (p.Asp294Asn)	NTN3 (D294N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528178	NM_006181.3(NTN3):c.907C>T (p.Arg303Trp)	NTN3 (R303W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403696	NM_006181.3(NTN3):c.961C>T (p.Arg321Cys)	NTN3 (R321C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202597	NM_006181.3(NTN3):c.970A>G (p.Met324Val)	NTN3 (M324V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331396	NM_006181.3(NTN3):c.1025G>A (p.Arg342Gln)	NTN3 (R342Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202588	NM_006181.3(NTN3):c.1061G>A (p.Arg354Gln)	NTN3 (R354Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305876	NM_006181.3(NTN3):c.1076G>A (p.Arg359Gln)	NTN3 (R359Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354024	NM_006181.3(NTN3):c.1088G>A (p.Arg363His)	NTN3 (R363H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301282	NM_006181.3(NTN3):c.1123G>A (p.Asp375Asn)	NTN3 (D375N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301283	NM_006181.3(NTN3):c.1217G>T (p.Arg406Leu)	NTN3 (R406L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3202590	NM_006181.3(NTN3):c.1217G>A (p.Arg406His)	NTN3 (R406H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213934	NM_006181.3(NTN3):c.1243C>T (p.Arg415Cys)	NTN3 (R415C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589390	NM_006181.3(NTN3):c.1256C>T (p.Ala419Val)	NTN3 (A419V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310986	NM_006181.3(NTN3):c.1313C>T (p.Pro438Leu)	NTN3 (P438L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225993	NM_006181.3(NTN3):c.1358G>T (p.Arg453Leu)	NTN3 (R453L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271113	NM_006181.3(NTN3):c.1373A>G (p.Lys458Arg)	NTN3 (K458R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535208	NM_006181.3(NTN3):c.1408G>A (p.Val470Met)	LOC130058242, NTN3 (V470M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343129	NM_006181.3(NTN3):c.1570C>A (p.Arg524Ser)	NTN3 (R524S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301285	NM_006181.3(NTN3):c.1606G>C (p.Ala536Pro)	LOC130058243, NTN3 (A536P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520820	NM_006181.3(NTN3):c.1609G>A (p.Gly537Arg)	LOC130058243, NTN3 (G537R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382324	NM_006181.3(NTN3):c.1621G>A (p.Gly541Ser)	LOC130058243, NTN3 (G541S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301284	NM_006181.3(NTN3):c.1642G>A (p.Ala548Thr)	LOC130058243, NTN3 (A548T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320264	NM_006181.3(NTN3):c.1648C>G (p.Arg550Gly)	NTN3 (R550G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520722	NM_006181.3(NTN3):c.1691G>C (p.Arg564Pro)	NTN3 (R564P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349396	NM_006181.3(NTN3):c.1723G>C (p.Gly575Arg)	LOC130058244, NTN3 (G575R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 47