"Ambry Genetics"[submitter] AND "NTN4"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2329275	NM_021229.4(NTN4):c.1615G>A (p.Gly539Ser)	NTN4 (G502S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2263150	NM_021229.4(NTN4):c.1535C>T (p.Thr512Ile)	NTN4 (T475I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2492402	NM_021229.4(NTN4):c.1528G>A (p.Glu510Lys)	NTN4 (E510K +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2227943	NM_021229.4(NTN4):c.1523G>A (p.Cys508Tyr)	NTN4 (C471Y +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2531324	NM_021229.4(NTN4):c.1481C>T (p.Ala494Val)	NTN4 (A494V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2297200	NM_021229.4(NTN4):c.1480G>A (p.Ala494Thr)	NTN4 (A494T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2525650	NM_021229.4(NTN4):c.1441G>T (p.Val481Leu)	NTN4 (V481L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2333639	NM_021229.4(NTN4):c.1340G>T (p.Arg447Leu)	NTN4 (R447L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2456199	NM_021229.4(NTN4):c.1289G>A (p.Arg430His)	NTN4 (R430H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2248222	NM_021229.4(NTN4):c.1048G>A (p.Ala350Thr)	NTN4 (A350T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2221011	NM_021229.4(NTN4):c.926C>T (p.Pro309Leu)	NTN4 (P272L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2545594	NM_021229.4(NTN4):c.858C>A (p.Phe286Leu)	NTN4 (F249L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2536368	NM_021229.4(NTN4):c.827G>A (p.Gly276Asp)	NTN4 (G276D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2386806	NM_021229.4(NTN4):c.802G>A (p.Ala268Thr)	NTN4 (A268T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2468435	NM_021229.4(NTN4):c.496G>A (p.Ala166Thr)	NTN4 (A129T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2365950	NM_021229.4(NTN4):c.298C>T (p.Arg100Trp)	NTN4 (R63W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2244897	NM_021229.4(NTN4):c.155C>T (p.Thr52Ile)	NTN4 (T15I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2409118	NM_021229.4(NTN4):c.100T>C (p.Cys34Arg)	NTN4 (C34R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2342139	NM_021229.4(NTN4):c.49G>A (p.Ala17Thr)	NTN4 (A17T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2529702	NM_021229.4(NTN4):c.8G>A (p.Ser3Asn)	NTN4 (S3N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 20