ClinVar for Gene (Select 159195) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3467273	NM_001391956.1(USP54):c.2738T>C (p.Met913Thr)	USP54 (M913T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3467272	NM_001391956.1(USP54):c.1786C>G (p.His596Asp)	USP54 (H596D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467271	NM_001391956.1(USP54):c.4603C>T (p.Arg1535Cys)	PPP3CB-AS1, USP54 (R1385C +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467270	NM_001391956.1(USP54):c.3577G>A (p.Gly1193Arg)	USP54 (G1043R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3467269	NM_001391956.1(USP54):c.4979G>A (p.Gly1660Glu)	PPP3CB-AS1, USP54 (G1556E +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3467268	NM_001391956.1(USP54):c.1300A>G (p.Ser434Gly)	USP54 (S434G +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3467267	NM_001391956.1(USP54):c.1440C>A (p.His480Gln)	USP54 (H423Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467266	NM_001391956.1(USP54):c.3190C>G (p.Pro1064Ala)	USP54 (P967A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467265	NM_001391956.1(USP54):c.4355G>A (p.Cys1452Tyr)	PPP3CB-AS1, USP54 (C1302Y +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467264	NM_001391956.1(USP54):c.680G>T (p.Ser227Ile)	USP54 (S227I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3467263	NM_001391956.1(USP54):c.2201A>G (p.Glu734Gly)	USP54 (E756G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467262	NM_001391956.1(USP54):c.4555G>A (p.Gly1519Arg)	PPP3CB-AS1, USP54 (G1541R +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467261	NM_001391956.1(USP54):c.1864C>T (p.Pro622Ser)	USP54 (P472S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467260	NM_001391956.1(USP54):c.2917G>A (p.Gly973Ser)	USP54 (G876S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467259	NM_001391956.1(USP54):c.3110C>T (p.Pro1037Leu)	USP54 (P980L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3467258	NM_001391956.1(USP54):c.3817C>A (p.Gln1273Lys)	USP54 (Q1273K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467257	NM_001391956.1(USP54):c.2021G>A (p.Ser674Asn)	LOC121815949, USP54 (S674N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467256	NM_001391956.1(USP54):c.4210G>A (p.Asp1404Asn)	PPP3CB-AS1, USP54 (D1307N +5 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3467255	NM_001391956.1(USP54):c.4238G>A (p.Arg1413His)	PPP3CB-AS1, USP54 (R1263H +5 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3467254	NM_001391956.1(USP54):c.2980G>A (p.Ala994Thr)	USP54 (A844T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3467253	NM_001391956.1(USP54):c.553A>G (p.Ile185Val)	USP54 (I185V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3467252	NM_001391956.1(USP54):c.2734G>A (p.Gly912Ser)	USP54 (G855S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331652	NM_001391956.1(USP54):c.3107C>T (p.Ser1036Phe)	USP54 (S1036F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331651	NM_001391956.1(USP54):c.3915T>A (p.His1305Gln)	USP54 (H1327Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331650	NM_001391956.1(USP54):c.3046G>C (p.Glu1016Gln)	USP54 (E1038Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331649	NM_001391956.1(USP54):c.4309T>A (p.Phe1437Ile)	PPP3CB-AS1, USP54 (F1287I +5 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3331648	NM_001391956.1(USP54):c.446A>G (p.His149Arg)	USP54 (H149R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3331647	NM_001391956.1(USP54):c.2255C>T (p.Ala752Val)	USP54 (A602V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331646	NM_001391956.1(USP54):c.2812C>G (p.Pro938Ala)	USP54 (P881A +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331645	NM_001391956.1(USP54):c.3341G>T (p.Ser1114Ile)	USP54 (S1057I +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331644	NM_001391956.1(USP54):c.2575C>T (p.Arg859Trp)	USP54 (R709W +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3331642	NM_001391956.1(USP54):c.1247C>T (p.Ser416Phe)	USP54 (S266F +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3331641	NM_001391956.1(USP54):c.1651C>A (p.His551Asn)	USP54 (H401N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331640	NM_001391956.1(USP54):c.4409G>A (p.Gly1470Asp)	PPP3CB-AS1, USP54 (G1413D +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331639	NM_001391956.1(USP54):c.3436G>A (p.Asp1146Asn)	USP54 (D1049N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331638	NM_001391956.1(USP54):c.3422G>A (p.Gly1141Asp)	USP54 (G1141D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331637	NM_001391956.1(USP54):c.4876T>C (p.Ser1626Pro)	PPP3CB-AS1, USP54 (S1569P +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331636	NM_001391956.1(USP54):c.1655C>T (p.Ser552Phe)	USP54 (S552F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3331635	NM_001391956.1(USP54):c.4345G>A (p.Gly1449Arg)	PPP3CB-AS1, USP54 (G1392R +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187801	NM_001391956.1(USP54):c.720G>C (p.Met240Ile)	USP54 (M262I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3187800	NM_001391956.1(USP54):c.696G>T (p.Arg232Ser)	USP54 (R232S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3187799	NM_001391956.1(USP54):c.587G>A (p.Cys196Tyr)	USP54 (C218Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3187798	NM_001391956.1(USP54):c.544G>A (p.Val182Ile)	USP54 (V182I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3187797	NM_001391956.1(USP54):c.4831C>A (p.His1611Asn)	PPP3CB-AS1, USP54 (H1507N +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187796	NM_001391956.1(USP54):c.4731G>T (p.Lys1577Asn)	PPP3CB-AS1, USP54 (K1599N +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187795	NM_001391956.1(USP54):c.4292C>T (p.Pro1431Leu)	PPP3CB-AS1, USP54 (P1453L +5 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3187793	NM_001391956.1(USP54):c.4213G>A (p.Glu1405Lys)	PPP3CB-AS1, USP54 (E1255K +5 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3187792	NM_001391956.1(USP54):c.4087G>C (p.Ala1363Pro)	PPP3CB-AS1, USP54 (A1385P +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3187791	NM_001391956.1(USP54):c.4084T>A (p.Ser1362Thr)	PPP3CB-AS1, USP54 (S1212T +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3187790	NM_001391956.1(USP54):c.4042A>G (p.Ser1348Gly)	USP54 (S1198G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187789	NM_001391956.1(USP54):c.392G>A (p.Arg131Lys)	USP54 (R131K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3187788	NM_001391956.1(USP54):c.381C>A (p.Asn127Lys)	USP54 (N127K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3187787	NM_001391956.1(USP54):c.35G>A (p.Arg12His)	USP54 (R12H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187786	NM_001391956.1(USP54):c.3593C>A (p.Ser1198Tyr)	USP54 (S1048Y +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187785	NM_001391956.1(USP54):c.3464T>C (p.Leu1155Ser)	USP54 (L1155S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187784	NM_001391956.1(USP54):c.2791G>C (p.Glu931Gln)	USP54 (E953Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187783	NM_001391956.1(USP54):c.268A>G (p.Ser90Gly)	USP54 (S90G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187782	NM_001391956.1(USP54):c.2624C>T (p.Ser875Leu)	USP54 (S875L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3187781	NM_001391956.1(USP54):c.2302G>A (p.Ala768Thr)	USP54 (A618T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187780	NM_001391956.1(USP54):c.1897C>A (p.Pro633Thr)	USP54 (P633T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187779	NM_001391956.1(USP54):c.1487C>T (p.Ser496Phe)	USP54 (S346F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187778	NM_001391956.1(USP54):c.1414G>A (p.Asp472Asn)	USP54 (D494N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3187777	NM_001391956.1(USP54):c.1088C>T (p.Pro363Leu)	USP54 (P213L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3045474	NM_001391956.1(USP54):c.2060+93G>C	LOC121815949, USP54 (G718A)	Single nucleotide variant (missense variant +1 more)	USP54-related disorder	GLikely benign
Select item 3044550	NM_001391956.1(USP54):c.4183C>T (p.Arg1395Ter)	PPP3CB-AS1, USP54 (R1245* +5 more)	Single nucleotide variant (non-coding transcript variant +2 more)	USP54-related disorder	GLikely benign
Select item 3038707	NM_001391956.1(USP54):c.331C>G (p.Gln111Glu)	USP54 (Q111E)	Single nucleotide variant (missense variant +1 more)	USP54-related disorder	GLikely benign
Select item 3038467	NM_001391956.1(USP54):c.4351C>T (p.Arg1451Cys)	PPP3CB-AS1, USP54 (R1301C +7 more)	Single nucleotide variant (missense variant +1 more)	USP54-related disorder	GLikely benign
Select item 2684602	GRCh37/hg19 10q11.21-24.2(chr10:42709645-100834951)x3	RRP12, RTKN2 +332 more	Copy number gain	not provided	GPathogenic
Select item 2640588	NM_001391956.1(USP54):c.2974T>C (p.Leu992=)	USP54	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2597897	NM_001391956.1(USP54):c.842C>T (p.Thr281Met)	USP54 (T131M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	AGAP5, CRTAC1 +682 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574686	GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	ABRAXAS2, CHCHD1 +673 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 2556708	NM_001391956.1(USP54):c.1658G>A (p.Arg553His)	USP54 (R496H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2555025	NM_001391956.1(USP54):c.4546A>G (p.Thr1516Ala)	PPP3CB-AS1, USP54 (T1412A +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554556	NM_001391956.1(USP54):c.163G>A (p.Asp55Asn)	USP54 (D55N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554021	NM_001391956.1(USP54):c.1208A>G (p.Lys403Arg)	USP54 (K253R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2553736	NM_001391956.1(USP54):c.4993C>G (p.Leu1665Val)	PPP3CB-AS1, USP54 (L1603V +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552501	NM_001391956.1(USP54):c.1970G>A (p.Arg657Gln)	USP54 (R600Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550710	NM_001391956.1(USP54):c.2621C>T (p.Pro874Leu)	USP54 (P724L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548106	NM_001391956.1(USP54):c.1925G>A (p.Arg642Gln)	USP54 (R492Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540352	NM_001391956.1(USP54):c.4717C>T (p.Pro1573Ser)	PPP3CB-AS1, USP54 (P1423S +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535368	NM_001391956.1(USP54):c.2632T>C (p.Ser878Pro)	USP54 (S728P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526589	NM_001391956.1(USP54):c.1543A>G (p.Met515Val)	USP54 (M365V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522268	NM_001391956.1(USP54):c.4732G>A (p.Gly1578Ser)	PPP3CB-AS1, USP54 (G1481S +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492391	NM_001391956.1(USP54):c.4390C>G (p.Pro1464Ala)	PPP3CB-AS1, USP54 (P1417A +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480975	NM_001391956.1(USP54):c.3037C>T (p.Pro1013Ser)	USP54 (P1013S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2475715	NM_001391956.1(USP54):c.3536G>A (p.Gly1179Asp)	USP54 (G1082D +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468691	NM_001391956.1(USP54):c.4082A>G (p.His1361Arg)	PPP3CB-AS1, USP54 (H1211R +4 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2459871	NM_001391956.1(USP54):c.4249C>T (p.Arg1417Cys)	PPP3CB-AS1, USP54 (R1360C +5 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided +1 more	GUncertain significance
Select item 2457106	NM_001391956.1(USP54):c.3875C>T (p.Thr1292Met)	USP54 (T1292M +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2455040	NM_001391956.1(USP54):c.1829C>T (p.Ala610Val)	USP54 (A460V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407549	NM_001391956.1(USP54):c.2104C>A (p.Arg702Ser)	USP54 (R702S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402492	NM_001391956.1(USP54):c.1022A>G (p.His341Arg)	USP54 (H191R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401848	NM_001391956.1(USP54):c.2873C>T (p.Ser958Leu)	USP54 (S861L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398018	NM_001391956.1(USP54):c.2452G>A (p.Ala818Thr)	USP54 (A840T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397455	NM_001391956.1(USP54):c.3630A>T (p.Leu1210Phe)	USP54 (L1232F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384265	NM_001391956.1(USP54):c.4217A>G (p.Gln1406Arg)	PPP3CB-AS1, USP54 (Q1309R +5 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2373340	NM_001391956.1(USP54):c.4604G>A (p.Arg1535His)	PPP3CB-AS1, USP54 (R1431H +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370218	NM_001391956.1(USP54):c.4027G>A (p.Ala1343Thr)	USP54 (A1286T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369306	NM_001391956.1(USP54):c.3835C>T (p.Pro1279Ser)	USP54 (P1129S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

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