NRXN2[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3301100	NM_015080.4(NRXN2):c.5087C>G (p.Pro1696Arg)	NRXN2 (P1502R +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 684468	NM_015080.4(NRXN2):c.5065A>C (p.Lys1689Gln)	NRXN2 (K1619Q +7 more)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 2505115	NM_015080.4(NRXN2):c.5038_5039del (p.Ser1680fs)	NRXN2 (S1449fs +9 more)	Deletion (frameshift variant)	Autism spectrum disorder +1 more	Gnot provided
Select item 2551753	NM_015080.4(NRXN2):c.4987C>T (p.Arg1663Cys)	NRXN2 (R1432C +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 975307	NM_015080.4(NRXN2):c.4985A>G (p.Asn1662Ser)	NRXN2 (N1431S +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 724994	NM_015080.4(NRXN2):c.4932G>A (p.Ala1644=)	NRXN2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3301103	NM_015080.4(NRXN2):c.4865C>T (p.Pro1622Leu)	NRXN2 (P1421L +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3301099	NM_015080.4(NRXN2):c.4862G>A (p.Gly1621Asp)	NRXN2 (G1419D +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245342	NM_015080.4(NRXN2):c.4861G>A (p.Gly1621Ser)	NRXN2 (G1390S +9 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 436043	NM_015080.4(NRXN2):c.4847G>T (p.Gly1616Val)	NRXN2 (G1546V +7 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 978883	NM_015080.4(NRXN2):c.4845dup (p.Gly1616fs)	NRXN2 (G1385fs +7 more)	Duplication (frameshift variant)	Intellectual disability	GUncertain significance
Select item 2534357	NM_015080.4(NRXN2):c.4823A>G (p.His1608Arg)	NRXN2 (H1608R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2489543	NM_015080.4(NRXN2):c.4813G>C (p.Gly1605Arg)	NRXN2 (G1535R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405920	NM_015080.4(NRXN2):c.4811C>T (p.Pro1604Leu)	NRXN2 (P558L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486173	NM_015080.4(NRXN2):c.4777C>A (p.Pro1593Thr)	NRXN2 (P1523T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534356	NM_015080.4(NRXN2):c.4651T>C (p.Phe1551Leu)	NRXN2 (F1481L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2235479	NM_015080.4(NRXN2):c.4625G>A (p.Gly1542Glu)	NRXN2 (G496E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 211710	NM_015080.4(NRXN2):c.4622A>T (p.Asp1541Val)	NRXN2 (D1471V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3061113	NM_015080.4(NRXN2):c.4601C>G (p.Pro1534Arg)	NRXN2 (P1464R +2 more)	Single nucleotide variant (missense variant +1 more)	NRXN2-related disorder	GUncertain significance
Select item 2468659	NM_015080.4(NRXN2):c.4595C>A (p.Pro1532His)	NRXN2 (P1532H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 436053	NM_015080.4(NRXN2):c.4519C>T (p.Pro1507Ser)	NRXN2 (P1437S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296653	NM_015080.4(NRXN2):c.4455C>A (p.Asp1485Glu)	NRXN2 (D1415E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2096493	NM_015080.4(NRXN2):c.4446C>G (p.Asp1482Glu)	NRXN2 (D436E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2689608	NM_015080.4(NRXN2):c.4444del (p.Asp1482fs)	NRXN2 (D1412fs +2 more)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 1679775	NM_015080.4(NRXN2):c.4440G>T (p.Glu1480Asp)	NRXN2 (E1410D +2 more)	Single nucleotide variant (missense variant +1 more)	NRXN2-related autism spectrum disorder	GUncertain significance
Select item 211709	NM_015080.4(NRXN2):c.4437C>T (p.Ala1479=)	NRXN2	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2530581	NM_015080.4(NRXN2):c.4415C>A (p.Pro1472His)	NRXN2 (P426H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202247	NM_015080.4(NRXN2):c.4391C>T (p.Pro1464Leu)	NRXN2 (P1394L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3301098	NM_015080.4(NRXN2):c.4361C>G (p.Thr1454Arg)	NRXN2 (T1384R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2443001	NM_015080.4(NRXN2):c.4323del (p.Phe1442fs)	NRXN2 (F1372fs +2 more)	Deletion (frameshift variant +1 more)	not provided	GUncertain significance
Select item 2629817	NM_015080.4(NRXN2):c.4259A>G (p.Glu1420Gly)	NRXN2 (E1350G +2 more)	Single nucleotide variant (missense variant +1 more)	NRXN2-related disorder	GUncertain significance
Select item 1226304	NM_015080.4(NRXN2):c.4253-203G>A	NRXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1213783	NM_015080.4(NRXN2):c.4249A>G (p.Thr1417Ala)	NRXN2 (T1347A +6 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 756811	NM_015080.4(NRXN2):c.4215C>T (p.Ser1405=)	NRXN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3345162	NM_015080.4(NRXN2):c.4187T>G (p.Leu1396Arg)	NRXN2 (L1326R +8 more)	Single nucleotide variant (missense variant)	NRXN2-related disorder	GUncertain significance
Select item 1259385	NM_015080.4(NRXN2):c.4174-88C>T	NRXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3202246	NM_015080.4(NRXN2):c.4162A>G (p.Ser1388Gly)	NRXN2 (S1373G +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1703152	NM_015080.4(NRXN2):c.4142G>A (p.Arg1381His)	NRXN2 (R1311H +8 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2320722	NM_015080.4(NRXN2):c.4096A>G (p.Met1366Val)	NRXN2 (M1351V +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216136	NM_015080.4(NRXN2):c.4058C>T (p.Thr1353Met)	NRXN2 (T1283M +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318320	NM_015080.4(NRXN2):c.4053G>T (p.Glu1351Asp)	NRXN2 (E1281D +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1337255	NM_015080.4(NRXN2):c.4046G>A (p.Ser1349Asn)	NRXN2 (S1279N +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 436044	NM_015080.4(NRXN2):c.4035C>T (p.Ser1345=)	NRXN2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3202245	NM_015080.4(NRXN2):c.4027G>A (p.Gly1343Arg)	NRXN2 (G218R +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 756802	NM_015080.4(NRXN2):c.4020G>C (p.Val1340=)	NRXN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2588642	NM_015080.4(NRXN2):c.3976G>A (p.Glu1326Lys)	NRXN2 (E1256K +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 211708	NM_015080.4(NRXN2):c.3965C>T (p.Ala1322Val)	NRXN2 (A1252V +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265611	NM_015080.4(NRXN2):c.3898C>T (p.Arg1300Trp)	NRXN2 (R1263W +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258631	NM_015080.4(NRXN2):c.3883A>T (p.Ile1295Phe)	NRXN2 (I1225F +8 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 129836	NM_015080.4(NRXN2):c.3851G>T (p.Arg1284Leu)	NRXN2 (R1214L +6 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 211707	NM_015080.4(NRXN2):c.3757+9C>T	NRXN2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 436045	NM_015080.4(NRXN2):c.3651C>T (p.Asn1217=)	NRXN2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3301102	NM_015080.4(NRXN2):c.3640G>C (p.Asp1214His)	NRXN2 (D89H +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1247078	NM_015080.4(NRXN2):c.3585+48A>G	NRXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 388809	NM_015080.4(NRXN2):c.3585C>A (p.Ile1195=)	NRXN2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2613458	NM_015080.4(NRXN2):c.3556G>A (p.Gly1186Ser)	NRXN2 (G1186S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 763458	NM_015080.4(NRXN2):c.3525C>T (p.Ser1175=)	NRXN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1341933	NM_015080.4(NRXN2):c.3410C>T (p.Thr1137Ile)	NRXN2 (T1097I +5 more)	Single nucleotide variant (missense variant)	Autism	GUncertain significance
Select item 1342509	NM_015080.4(NRXN2):c.3406G>A (p.Gly1136Arg)	NRXN2 (G1096R +5 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 560283	NM_015080.4(NRXN2):c.3403+5509C>T	NRXN2 (P32S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3353989	NM_015080.4(NRXN2):c.3403+5489C>T	NRXN2 (P25L)	Single nucleotide variant (missense variant +1 more)	NRXN2-related disorder	GUncertain significance
Select item 2631543	NM_015080.4(NRXN2):c.3403+1G>A	NRXN2	Single nucleotide variant (splice donor variant)	NRXN2-related disorder	GUncertain significance
Select item 211706	NM_015080.4(NRXN2):c.3403C>T (p.Pro1135Ser)	NRXN2 (P1095S +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 436054	NM_015080.4(NRXN2):c.3368C>T (p.Thr1123Ile)	NRXN2 (T1083I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 129835	NM_015080.4(NRXN2):c.3327C>T (p.Gly1109=)	NRXN2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1253337	NM_015080.4(NRXN2):c.3284-93G>A	NRXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232789	NM_015080.4(NRXN2):c.3283+175G>T	NRXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1489457	NM_015080.4(NRXN2):c.3256A>G (p.Ile1086Val)	NRXN2 (I1079V +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2322507	NM_015080.4(NRXN2):c.3254G>T (p.Arg1085Leu)	NRXN2 (R1045L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 978098	NM_015080.4(NRXN2):c.3254G>A (p.Arg1085His)	NRXN2 (R1045H +4 more)	Single nucleotide variant (missense variant)	NRXN2-associated Neurodevelopmental disorder	GUncertain significance
Select item 2234006	NM_015080.4(NRXN2):c.3244G>T (p.Ala1082Ser)	NRXN2 (A1042S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 436046	NM_015080.4(NRXN2):c.3228A>G (p.Pro1076=)	NRXN2	Single nucleotide variant (synonymous variant)	not specified	GUncertain significance
Select item 2257699	NM_015080.4(NRXN2):c.3217G>A (p.Gly1073Arg)	NRXN2 (G1058R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 211705	NM_015080.4(NRXN2):c.3213C>G (p.Leu1071=)	NRXN2	Single nucleotide variant (synonymous variant)	not specified	GBenign
Select item 599182	NM_015080.4(NRXN2):c.3176G>A (p.Arg1059Gln)	NRXN2 (R1059Q +4 more)	Single nucleotide variant (missense variant)	Developmental and epileptic encephalopathy, 1	GUncertain significance
Select item 129834	NM_015080.4(NRXN2):c.3133A>G (p.Ser1045Gly)	NRXN2 (S1005G +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2257113	NM_015080.4(NRXN2):c.3061C>T (p.Arg1021Cys)	NRXN2 (R1006C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2634931	NM_015080.4(NRXN2):c.3059C>T (p.Ser1020Phe)	NRXN2 (S1005F +4 more)	Single nucleotide variant (missense variant)	NRXN2-related disorder	GUncertain significance
Select item 2471328	NM_015080.4(NRXN2):c.3037G>A (p.Val1013Met)	NRXN2 (V998M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1258956	NM_015080.4(NRXN2):c.2919-149A>G	NRXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230516	NM_015080.4(NRXN2):c.2919-195C>T	NRXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 211704	NM_015080.4(NRXN2):c.2918+6G>A	NRXN2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 2547868	NM_015080.4(NRXN2):c.2905G>A (p.Glu969Lys)	NRXN2 (E962K +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 211703	NM_015080.4(NRXN2):c.2883C>T (p.Asn961=)	NRXN2	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 129833	NM_015080.4(NRXN2):c.2745C>T (p.Ile915=)	NRXN2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2370117	NM_015080.4(NRXN2):c.2738G>A (p.Arg913His)	NRXN2 (R905H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3239591	NM_015080.4(NRXN2):c.2708A>G (p.Tyr903Cys)	NRXN2 (Y863C +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 734619	NM_015080.4(NRXN2):c.2697T>G (p.Gly899=)	NRXN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 211702	NM_015080.4(NRXN2):c.2677A>G (p.Met893Val)	NRXN2 (M853V +4 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 732862	NM_015080.4(NRXN2):c.2656G>A (p.Val886Met)	NRXN2 (V871M +4 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2636894	NM_015080.4(NRXN2):c.2606G>A (p.Arg869Gln)	NRXN2 (R829Q +4 more)	Single nucleotide variant (missense variant)	NRXN2-related disorder	GUncertain significance
Select item 2524447	NM_015080.4(NRXN2):c.2605C>T (p.Arg869Trp)	NRXN2 (R854W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206679	NM_015080.4(NRXN2):c.2585C>T (p.Thr862Met)	NRXN2 (T854M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 211701	NM_015080.4(NRXN2):c.2537-8C>T	NRXN2	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 1280367	NM_015080.4(NRXN2):c.2537-109A>C	NRXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236422	NM_015080.4(NRXN2):c.2537-110A>G	NRXN2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2689610	NM_015080.4(NRXN2):c.2515G>C (p.Val839Leu)	NRXN2 (V799L +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 211700	NM_015080.4(NRXN2):c.2463T>C (p.Asn821=)	NRXN2	Single nucleotide variant (synonymous variant)	not specified	GUncertain significance
Select item 2463018	NM_015080.4(NRXN2):c.2456A>G (p.Asn819Ser)	NRXN2 (N779S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247932	NM_015080.4(NRXN2):c.2447A>G (p.His816Arg)	NRXN2 (H801R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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