NRAP[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1274061	NM_198060.4(NRAP):c.5088+27del	NRAP	Deletion (intron variant)	not provided	GBenign
Select item 3050126	NM_198060.4(NRAP):c.5088+1G>A	NRAP	Single nucleotide variant (splice donor variant)	NRAP-related disorder	GLikely benign
Select item 3038468	NM_198060.4(NRAP):c.5051T>A (p.Leu1684Gln)	NRAP (L1648Q +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GLikely benign
Select item 768389	NM_198060.4(NRAP):c.5046G>A (p.Ala1682=)	NRAP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2615232	NM_198060.4(NRAP):c.5039G>C (p.Arg1680Pro)	NRAP (R1644P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1258525	NM_198060.4(NRAP):c.4956+194C>T	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 776544	NM_198060.4(NRAP):c.4927G>T (p.Ala1643Ser)	NRAP (A1608S +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1257443	NM_198060.4(NRAP):c.4905G>A (p.Pro1635=)	NRAP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2596147	NM_198060.4(NRAP):c.4904C>T (p.Pro1635Leu)	NRAP (P1599L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240889	NM_198060.4(NRAP):c.4856C>A (p.Ala1619Asp)	NRAP (A1583D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231718	NM_198060.4(NRAP):c.4802A>C (p.His1601Pro)	NRAP (H1565P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3202014	NM_198060.4(NRAP):c.4769A>G (p.Lys1590Arg)	NRAP (K1590R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3202013	NM_198060.4(NRAP):c.4764G>C (p.Glu1588Asp)	NRAP (E1552D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3202012	NM_198060.4(NRAP):c.4738G>A (p.Val1580Ile)	NRAP (V1545I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2389836	NM_198060.4(NRAP):c.4708G>A (p.Asp1570Asn)	NRAP (D1535N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236321	NM_198060.4(NRAP):c.4705G>A (p.Asp1569Asn)	NRAP (D1534N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2236320	NM_198060.4(NRAP):c.4699A>G (p.Ser1567Gly)	NRAP (S1531G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2640847	NM_198060.4(NRAP):c.4676G>C (p.Arg1559Pro)	NRAP (R1523P +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2598916	NM_198060.4(NRAP):c.4676G>A (p.Arg1559Gln)	NRAP (R1524Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3354012	NM_198060.4(NRAP):c.4648C>T (p.Arg1550Trp)	NRAP (R1514W +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GLikely benign
Select item 1229195	NM_198060.4(NRAP):c.4645-152A>G	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236724	NM_198060.4(NRAP):c.4592T>C (p.Leu1531Pro)	NRAP (L1495P +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2595031	NM_198060.4(NRAP):c.4562A>G (p.Gln1521Arg)	NRAP (Q1521R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1279036	NM_198060.4(NRAP):c.4537-107G>A	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236570	NM_198060.4(NRAP):c.4537-203G>A	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280246	NM_198060.4(NRAP):c.4536+208dup	NRAP	Duplication (intron variant)	not provided	GBenign
Select item 1249067	NM_198060.4(NRAP):c.4536+187T>C	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226674	NM_198060.4(NRAP):c.4536+54T>C	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3060628	NM_198060.4(NRAP):c.4536C>T (p.Asp1512=)	NRAP	Single nucleotide variant (synonymous variant)	NRAP-related disorder	GBenign
Select item 1320507	NM_198060.4(NRAP):c.4504C>T (p.Arg1502Ter)	NRAP (R1466* +2 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2247931	NM_198060.4(NRAP):c.4465C>A (p.His1489Asn)	NRAP (H1489N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2672417	NM_198060.4(NRAP):c.4433G>A (p.Arg1478His)	NRAP (R1442H +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1265735	NM_198060.4(NRAP):c.4431+169T>G	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3202011	NM_198060.4(NRAP):c.4415A>G (p.Tyr1472Cys)	NRAP (Y1436C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2383695	NM_198060.4(NRAP):c.4362C>G (p.Ile1454Met)	NRAP (I1419M +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1294904	NM_198060.4(NRAP):c.4333-135C>T	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1175644	NM_198060.4(NRAP):c.4333-189del	NRAP	Deletion (intron variant)	not provided	GBenign
Select item 734954	NM_198060.4(NRAP):c.4330G>A (p.Glu1444Lys)	NRAP (E1409K +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2520297	NM_198060.4(NRAP):c.4327A>G (p.Ser1443Gly)	NRAP (S1407G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3202009	NM_198060.4(NRAP):c.4321C>T (p.Leu1441Phe)	NRAP (L1405F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3202008	NM_198060.4(NRAP):c.4286C>A (p.Ser1429Tyr)	NRAP (S1394Y +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3202007	NM_198060.4(NRAP):c.4213G>T (p.Ala1405Ser)	NRAP (A1370S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2612157	NM_198060.4(NRAP):c.4172T>C (p.Leu1391Pro)	NRAP (L1355P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 718630	NM_198060.4(NRAP):c.4137C>T (p.His1379=)	NRAP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2631465	NM_198060.4(NRAP):c.4078C>T (p.Pro1360Ser)	NRAP (P1324S +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GUncertain significance
Select item 3350502	NM_198060.4(NRAP):c.4043G>A (p.Arg1348Lys)	NRAP (R1312K +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GLikely benign
Select item 2246940	NM_198060.4(NRAP):c.4030C>G (p.Leu1344Val)	NRAP (L1308V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2640848	NM_198060.4(NRAP):c.4010T>C (p.Met1337Thr)	NRAP (M1301T +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3354628	NM_198060.4(NRAP):c.4009A>G (p.Met1337Val)	NRAP (M1301V +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GUncertain significance
Select item 2260033	NM_198060.4(NRAP):c.3965C>G (p.Pro1322Arg)	NRAP (P1286R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2537399	NM_198060.4(NRAP):c.3962G>A (p.Gly1321Glu)	NRAP (G1321E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602999	NM_198060.4(NRAP):c.3905T>C (p.Ile1302Thr)	NRAP (I1266T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 994436	NM_198060.4(NRAP):c.3889C>G (p.Arg1297Gly)	NRAP (R1261G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 977178	NM_198060.4(NRAP):c.3866A>G (p.Glu1289Gly)	NRAP (E1253G +2 more)	Single nucleotide variant (missense variant)	Sudden unexplained death	GUncertain significance
Select item 2214327	NM_198060.4(NRAP):c.3847G>A (p.Gly1283Ser)	NRAP (G1247S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3045409	NM_198060.4(NRAP):c.3808G>A (p.Ala1270Thr)	NRAP (A1234T +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GLikely benign
Select item 778474	NM_198060.4(NRAP):c.3728A>T (p.Asp1243Val)	NRAP (D1207V +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2259824	NM_198060.4(NRAP):c.3722G>A (p.Gly1241Glu)	NRAP (G1205E +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2441828	NM_198060.4(NRAP):c.3703-1G>T	NRAP	Single nucleotide variant (splice acceptor variant)	Primary dilated cardiomyopathy	GUncertain significance
Select item 2681445	NM_198060.4(NRAP):c.3703-5C>T	NRAP	Single nucleotide variant (intron variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2281847	NM_198060.4(NRAP):c.3649A>G (p.Thr1217Ala)	NRAP (T1182A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3300989	NM_198060.4(NRAP):c.3643G>A (p.Ala1215Thr)	NRAP (A1179T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3202006	NM_198060.4(NRAP):c.3613C>T (p.Arg1205Trp)	NRAP (R1169W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2080715	NM_198060.4(NRAP):c.3604-2A>C	NRAP	Single nucleotide variant (splice acceptor variant)	not provided	GLikely pathogenic
Select item 1264742	NM_198060.4(NRAP):c.3603+206del	NRAP	Deletion (intron variant)	not provided	GBenign
Select item 1237400	NM_198060.4(NRAP):c.3603+86dup	NRAP	Duplication (intron variant)	not provided	GBenign
Select item 1182004	NM_198060.4(NRAP):c.3567T>C (p.Ile1189=)	NRAP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1182171	NM_198060.4(NRAP):c.3547A>G (p.Ile1183Val)	NRAP (I1147V +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2598927	NM_198060.4(NRAP):c.3508C>T (p.Arg1170Trp)	NRAP (R1134W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1280649	NM_198060.4(NRAP):c.3498+120C>A	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2246939	NM_198060.4(NRAP):c.3482A>T (p.His1161Leu)	NRAP (H1125L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3202005	NM_198060.4(NRAP):c.3466T>G (p.Cys1156Gly)	NRAP (C1120G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348927	NM_198060.4(NRAP):c.3454C>G (p.Leu1152Val)	NRAP (L1116V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3300988	NM_198060.4(NRAP):c.3436A>G (p.Thr1146Ala)	NRAP (T1110A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2242800	NM_198060.4(NRAP):c.3392C>A (p.Thr1131Asn)	NRAP (T1096N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3055247	NM_198060.4(NRAP):c.3335C>T (p.Ala1112Val)	NRAP (A1076V +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GBenign
Select item 3054715	NM_198060.4(NRAP):c.3314A>G (p.Lys1105Arg)	NRAP (K1069R +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GUncertain significance
Select item 1699323	NM_198060.4(NRAP):c.3301-2A>G	NRAP	Single nucleotide variant (splice acceptor variant)	Cardiomyopathy	GLikely pathogenic
Select item 1275958	NM_198060.4(NRAP):c.3300+184G>A	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282992	NM_198060.4(NRAP):c.3300+91A>G	NRAP	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3055529	NM_198060.4(NRAP):c.3300+8G>C	NRAP	Single nucleotide variant (intron variant)	NRAP-related disorder	GBenign
Select item 2493228	NM_198060.4(NRAP):c.3284C>A (p.Thr1095Asn)	NRAP (T1095N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3042091	NM_198060.4(NRAP):c.3239G>A (p.Arg1080Gln)	NRAP (R1044Q +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GLikely benign
Select item 3037480	NM_198060.4(NRAP):c.3207T>A (p.Phe1069Leu)	NRAP (F1033L +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GLikely benign
Select item 2446264	NM_198060.4(NRAP):c.3186+3G>C	NRAP	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 785811	NM_198060.4(NRAP):c.3163G>A (p.Ala1055Thr)	NRAP (A1019T +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2611231	NM_198060.4(NRAP):c.3137A>G (p.Asp1046Gly)	NRAP (D1010G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1279354	NM_198060.4(NRAP):c.3114T>C (p.Asp1038=)	NRAP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2579962	NM_198060.4(NRAP):c.3109C>T (p.Arg1037Ter)	NRAP (R1001* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 2227634	NM_198060.4(NRAP):c.3083G>A (p.Arg1028His)	NRAP (R1028H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 716417	NM_198060.4(NRAP):c.3064A>G (p.Met1022Val)	NRAP (M1022V +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1277156	NM_198060.4(NRAP):c.3021G>T (p.Pro1007=)	NRAP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3043210	NM_198060.4(NRAP):c.3011A>G (p.His1004Arg)	NRAP (H1004R +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GBenign
Select item 2347924	NM_198060.4(NRAP):c.3007C>T (p.His1003Tyr)	NRAP (H968Y +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 710939	NM_198060.4(NRAP):c.2963A>C (p.Gln988Pro)	NRAP (Q988P +2 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 744340	NM_198060.4(NRAP):c.2940C>G (p.Val980=)	NRAP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2218505	NM_198060.4(NRAP):c.2930C>G (p.Pro977Arg)	NRAP (P977R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3045820	NM_198060.4(NRAP):c.2929C>T (p.Pro977Ser)	NRAP (P941S +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GLikely benign
Select item 2635670	NM_198060.4(NRAP):c.2903T>G (p.Leu968Trp)	NRAP (L932W +2 more)	Single nucleotide variant (missense variant)	NRAP-related disorder	GUncertain significance
Select item 1276145	NM_198060.4(NRAP):c.2897A>G (p.Asp966Gly)	NRAP (D930G +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign

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