"Ambry Genetics"[submitter] AND "NRXN3"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2369711	NM_001330195.2(NRXN3):c.1282A>T (p.Thr428Ser)	LOC105370589, NRXN3 (T432S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507672	NM_001330195.2(NRXN3):c.1303G>A (p.Glu435Lys)	LOC105370589, NRXN3 (E435K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514751	NM_001330195.2(NRXN3):c.1668A>G (p.Ile556Met)	NRXN3 (I560M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471363	NM_001330195.2(NRXN3):c.2322C>A (p.Asn774Lys)	NRXN3 (N401K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202253	NM_001330195.2(NRXN3):c.2348G>A (p.Arg783Gln)	NRXN3 (R410Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353090	NM_001330195.2(NRXN3):c.2382T>A (p.Asp794Glu)	NRXN3 (D421E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353091	NM_001330195.2(NRXN3):c.2383G>A (p.Asp795Asn)	NRXN3 (D422N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202254	NM_001330195.2(NRXN3):c.2464C>T (p.Arg822Cys)	NRXN3 (R449C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202255	NM_001330195.2(NRXN3):c.2537T>C (p.Ile846Thr)	NRXN3 (I850T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202256	NM_001330195.2(NRXN3):c.2650C>T (p.Leu884Phe)	NRXN3 (L511F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306830	NM_001330195.2(NRXN3):c.2809G>A (p.Gly937Ser)	NRXN3 (G941S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590069	NM_001330195.2(NRXN3):c.2840G>A (p.Arg947His)	NRXN3 (R947H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202257	NM_001330195.2(NRXN3):c.2843C>T (p.Pro948Leu)	NRXN3 (P575L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596711	NM_001330195.2(NRXN3):c.3080G>A (p.Arg1027His)	NRXN3 (R1027H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367964	NM_001330195.2(NRXN3):c.3131G>A (p.Arg1044His)	NRXN3 (R1044H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202258	NM_001330195.2(NRXN3):c.3340C>T (p.Arg1114Trp)	NRXN3 (R109W +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408862	NM_001330195.2(NRXN3):c.3607T>C (p.Tyr1203His)	NRXN3 (Y1207H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224691	NM_001330195.2(NRXN3):c.3871C>T (p.Arg1291Trp)	NRXN3 (R1291W +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314861	NM_001330195.2(NRXN3):c.3914C>T (p.Thr1305Met)	NRXN3 (T1309M +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202259	NM_001330195.2(NRXN3):c.3989A>C (p.Lys1330Thr)	NRXN3 (K295T +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302630	NM_001330195.2(NRXN3):c.3995G>A (p.Arg1332His)	NRXN3 (R1302H +5 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2293802	NM_001330195.2(NRXN3):c.4019C>A (p.Thr1340Lys)	NRXN3 (T335K +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202260	NM_001330195.2(NRXN3):c.4486A>T (p.Thr1496Ser)	NRXN3 (T986S +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308507	NM_001330195.2(NRXN3):c.4502G>C (p.Gly1501Ala)	NRXN3 (G1398A +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293878	NM_001330195.2(NRXN3):c.4696G>A (p.Asp1566Asn)	NRXN3 (D454N +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 25