ClinVar for Gene (Select 55280) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3378094	NM_018294.6(CWF19L1):c.1426A>G (p.Lys476Glu)	CWF19L1 (K231E +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3352139	NM_018294.6(CWF19L1):c.23+10C>G	CWF19L1	Single nucleotide variant (5 prime UTR variant +1 more)	CWF19L1-related disorder	GLikely benign
Select item 3270379	NM_018294.6(CWF19L1):c.1344G>T (p.Leu448Phe)	CWF19L1 (L203F +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3270378	NM_018294.6(CWF19L1):c.878A>C (p.Asp293Ala)	CWF19L1 (D293A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3270377	NM_018294.6(CWF19L1):c.1102A>G (p.Ile368Val)	CWF19L1 (I231V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3270376	NM_018294.6(CWF19L1):c.481G>A (p.Val161Met)	CWF19L1 (V161M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3270375	NM_018294.6(CWF19L1):c.8A>G (p.Gln3Arg)	CWF19L1 (Q3R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3256766	NM_018294.6(CWF19L1):c.1552G>A (p.Glu518Lys)	CWF19L1, CHUK-DT (E273K +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Autosomal recessive spinocerebellar ataxia 17	GLikely pathogenic
Select item 3079114	NM_018294.6(CWF19L1):c.931T>C (p.Ser311Pro)	CWF19L1 (S174P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079113	NM_018294.6(CWF19L1):c.905G>A (p.Arg302His)	CWF19L1 (R165H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079112	NM_018294.6(CWF19L1):c.84T>G (p.Ile28Met)	CWF19L1 (I28M)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3079110	NM_018294.6(CWF19L1):c.746T>C (p.Met249Thr)	CWF19L1 (M112T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3079109	NM_018294.6(CWF19L1):c.664C>T (p.Arg222Trp)	CWF19L1 (R222W +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3079108	NM_018294.6(CWF19L1):c.597G>T (p.Lys199Asn)	CWF19L1 (K199N +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3079107	NM_018294.6(CWF19L1):c.417G>A (p.Met139Ile)	CWF19L1 (M139I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3079106	NM_018294.6(CWF19L1):c.117G>T (p.Leu39Phe)	CWF19L1 (L39F)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3063164	GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3	ABCC2, ABLIM1 +293 more	Copy number gain	not specified	GPathogenic
Select item 3056968	NM_018294.6(CWF19L1):c.1568G>A (p.Arg523His)	CHUK-DT, CWF19L1 (R278H +3 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Autosomal recessive spinocerebellar ataxia 17	GBenign
Select item 3055889	NM_018294.6(CWF19L1):c.900G>A (p.Arg300=)	CWF19L1	Single nucleotide variant (synonymous variant)	CWF19L1-related disorder	GBenign
Select item 3052789	NM_018294.6(CWF19L1):c.249T>C (p.Asp83=)	CWF19L1	Single nucleotide variant (synonymous variant +2 more)	CWF19L1-related disorder	GLikely benign
Select item 3049798	NM_018294.6(CWF19L1):c.580T>C (p.Phe194Leu)	CWF19L1 (F194L +1 more)	Single nucleotide variant (missense variant +1 more)	CWF19L1-related disorder	GLikely benign
Select item 3046074	NM_018294.6(CWF19L1):c.792C>T (p.Asn264=)	CWF19L1	Single nucleotide variant (synonymous variant)	CWF19L1-related disorder	GLikely benign
Select item 3034201	NM_018294.6(CWF19L1):c.1152G>A (p.Glu384=)	CWF19L1	Single nucleotide variant (synonymous variant)	CWF19L1-related disorder	GLikely benign
Select item 2682516	NM_018294.6(CWF19L1):c.1037G>T (p.Gly346Val)	CWF19L1 (G101V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2629563	NM_018294.6(CWF19L1):c.108+1G>A	CWF19L1	Single nucleotide variant (intron variant +1 more)	CWF19L1-related disorder	GLikely pathogenic
Select item 2618199	NM_018294.6(CWF19L1):c.277A>G (p.Ile93Val)	CWF19L1 (I93V)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2578621	NM_018294.6(CWF19L1):c.964C>T (p.Pro322Ser)	CWF19L1 (P185S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2578620	NM_018294.6(CWF19L1):c.1543A>G (p.Lys515Glu)	CHUK-DT, CWF19L1 (K270E +3 more)	Single nucleotide variant (missense variant)	not provided	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 2551393	NM_018294.6(CWF19L1):c.82A>T (p.Ile28Phe)	CWF19L1 (I28F)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2550804	NM_018294.6(CWF19L1):c.1262C>T (p.Pro421Leu)	CWF19L1 (P284L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2541005	NM_018294.6(CWF19L1):c.512T>A (p.Val171Glu)	CWF19L1 (V34E +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2523678	NM_018294.6(CWF19L1):c.557C>T (p.Thr186Met)	CWF19L1 (T186M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2497675	NM_018294.6(CWF19L1):c.1375-2A>G	CWF19L1	Single nucleotide variant (splice acceptor variant)	Autosomal recessive spinocerebellar ataxia 17	GPathogenic
Select item 2497673	NM_018294.6(CWF19L1):c.452T>G (p.Ile151Ser)	CWF19L1 (I14S +1 more)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive spinocerebellar ataxia 17	GLikely pathogenic
Select item 2483287	NM_018294.6(CWF19L1):c.1283C>T (p.Thr428Ile)	CWF19L1 (T183I +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2482162	NM_018294.6(CWF19L1):c.7C>G (p.Gln3Glu)	CWF19L1 (Q3E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2470427	NM_018294.6(CWF19L1):c.818C>T (p.Ala273Val)	CWF19L1 (A28V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2429271	NM_018294.6(CWF19L1):c.1045-2A>C	CWF19L1	Single nucleotide variant (splice acceptor variant)	Autosomal recessive spinocerebellar ataxia 17	GLikely pathogenic
Select item 2424090	NC_000010.10:g.(?_99344461)_(105992004_?)dup	CPN1, CRTAC1 +95 more	Duplication	not provided	GUncertain significance
Select item 2407270	NM_018294.6(CWF19L1):c.667T>C (p.Phe223Leu)	CWF19L1 (F223L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2355031	NM_018294.6(CWF19L1):c.574T>C (p.Tyr192His)	CWF19L1 (Y55H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2352973	NM_018294.6(CWF19L1):c.313A>C (p.Ser105Arg)	CWF19L1 (S105R)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2351552	NM_018294.6(CWF19L1):c.293G>A (p.Arg98His)	CWF19L1 (R98H)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2347432	NM_018294.6(CWF19L1):c.1043A>G (p.His348Arg)	CWF19L1 (H103R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2331325	NM_018294.6(CWF19L1):c.682A>G (p.Asn228Asp)	CWF19L1 (N228D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2328886	NM_018294.6(CWF19L1):c.1390G>A (p.Ala464Thr)	CWF19L1 (A219T +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315754	NM_018294.6(CWF19L1):c.122T>C (p.Val41Ala)	CWF19L1 (V41A)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2307112	NM_018294.6(CWF19L1):c.540G>C (p.Leu180Phe)	CWF19L1 (L180F +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2284857	NM_018294.6(CWF19L1):c.823A>G (p.Ile275Val)	CWF19L1 (I138V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2281378	NM_018294.6(CWF19L1):c.1267C>G (p.Pro423Ala)	CWF19L1 (P178A +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2239882	NM_018294.6(CWF19L1):c.917G>A (p.Gly306Asp)	CWF19L1 (G306D +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231065	NM_018294.6(CWF19L1):c.694C>A (p.Pro232Thr)	CWF19L1 (P232T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2230721	NM_018294.6(CWF19L1):c.326A>C (p.Gln109Pro)	CWF19L1 (Q109P)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2229337	NM_018294.6(CWF19L1):c.922G>C (p.Asp308His)	CWF19L1 (D308H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2220631	NM_018294.6(CWF19L1):c.1571G>A (p.Arg524His)	CHUK-DT, CWF19L1 (R279H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1801967	NM_018294.6(CWF19L1):c.118T>C (p.Cys40Arg)	CWF19L1 (C40R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 1711160	NM_018294.6(CWF19L1):c.820dup (p.Ser274fs)	CWF19L1 (S137fs +2 more)	Duplication (frameshift variant)	Autosomal recessive spinocerebellar ataxia 17	GLikely pathogenic
Select item 1711159	NM_018294.6(CWF19L1):c.1394C>T (p.Ala465Val)	CWF19L1 (A220V +3 more)	Single nucleotide variant (missense variant)	Autosomal recessive spinocerebellar ataxia 17	GUncertain significance
Select item 1711123	NM_018294.6(CWF19L1):c.1070G>T (p.Gly357Val)	CWF19L1 (G112V +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive spinocerebellar ataxia 17	GPathogenic
Select item 1685293	NM_018294.6(CWF19L1):c.187+1G>T	CWF19L1	Single nucleotide variant (intron variant +1 more)	Autosomal recessive spinocerebellar ataxia 17	GLikely pathogenic
Select item 1678624	NM_018294.6(CWF19L1):c.1063A>G (p.Lys355Glu)	CWF19L1 (K110E +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive spinocerebellar ataxia 17	GUncertain significance
Select item 1678602	NM_018294.6(CWF19L1):c.1523G>A (p.Trp508Ter)	CHUK-DT, CWF19L1 (W263* +3 more)	Single nucleotide variant (nonsense)	Autosomal recessive spinocerebellar ataxia 17	GUncertain significance
Select item 1675429	NM_018294.6(CWF19L1):c.612del (p.Arg204fs)	CWF19L1 (R204fs +1 more)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 1675428	NM_018294.6(CWF19L1):c.1381C>T (p.Gln461Ter)	CWF19L1 (Q216* +3 more)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
Select item 1322180	NM_018294.6(CWF19L1):c.520A>T (p.Lys174Ter)	CWF19L1 (K174* +1 more)	Single nucleotide variant (nonsense +1 more)	Autosomal recessive spinocerebellar ataxia 17	GPathogenic
Select item 1016517	NM_018294.6(CWF19L1):c.23+6T>C	CWF19L1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 996893	NM_018294.6(CWF19L1):c.708+294_1044+1540del	CWF19L1	Deletion (splice acceptor variant +2 more)	Autosomal recessive spinocerebellar ataxia 17	GPathogenic
Select item 996587	NM_018294.6(CWF19L1):c.949C>T (p.Gln317Ter)	CWF19L1 (Q180* +2 more)	Single nucleotide variant (nonsense)	Intellectual disability	GLikely pathogenic
Select item 987461	NM_018294.6(CWF19L1):c.708+1G>A	CWF19L1	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 984934	NM_018294.6(CWF19L1):c.349G>T (p.Glu117Ter)	CWF19L1 (E117*)	Single nucleotide variant (nonsense +2 more)	Autosomal recessive spinocerebellar ataxia 17	GLikely pathogenic
Select item 981166	NM_018294.6(CWF19L1):c.1045T>G (p.Cys349Gly)	CWF19L1 (C104G +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive spinocerebellar ataxia 17	GUncertain significance
Select item 976766	NM_018294.6(CWF19L1):c.665G>A (p.Arg222Gln)	CWF19L1 (R222Q +1 more)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive spinocerebellar ataxia 17	GLikely pathogenic
Select item 976765	NM_018294.6(CWF19L1):c.1114C>T (p.Gln372Ter)	CWF19L1 (Q127* +2 more)	Single nucleotide variant (nonsense)	Autosomal recessive spinocerebellar ataxia 17	GPathogenic
Select item 872772	NM_018294.6(CWF19L1):c.37G>C (p.Asp13His)	CWF19L1 (D13H)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely pathogenic
Select item 872771	NM_018294.6(CWF19L1):c.943C>T (p.Pro315Ser)	CWF19L1 (P315S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 815373	GRCh37/hg19 10q24.31(chr10:101932457-102392841)x3	WNT8B, NDUFB8 +9 more	Copy number gain	not provided	GUncertain significance
Select item 813893	NM_018294.6(CWF19L1):c.1158dup (p.Lys387fs)	CWF19L1 (K142fs +2 more)	Duplication (frameshift variant)	Autosomal recessive spinocerebellar ataxia 17	GLikely pathogenic
Select item 806557	NM_018294.6(CWF19L1):c.942del (p.Pro315fs)	CWF19L1 (P178fs +2 more)	Deletion (frameshift variant)	Autosomal recessive spinocerebellar ataxia 17 +1 more	GLikely pathogenic
Select item 800879	NM_018294.6(CWF19L1):c.605dup (p.Tyr202Ter)	CWF19L1 (Y202* +1 more)	Duplication (nonsense +1 more)	Autosomal recessive spinocerebellar ataxia 17	GPathogenic
Select item 799371	NM_018294.6(CWF19L1):c.105T>C (p.Phe35=)	CWF19L1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 792283	NM_018294.6(CWF19L1):c.1374+8A>G	CWF19L1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 787543	NM_018294.6(CWF19L1):c.1255-7C>A	CWF19L1	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 768383	NM_018294.6(CWF19L1):c.1577G>A (p.Arg526Gln)	CHUK-DT, CWF19L1 (R486Q +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 759923	NM_018294.6(CWF19L1):c.615T>G (p.Leu205=)	CWF19L1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 743502	NM_018294.6(CWF19L1):c.1374+7C>A	CWF19L1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 741521	NM_018294.6(CWF19L1):c.437T>A (p.Phe146Tyr)	CWF19L1 (F146Y +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 737842	NM_018294.6(CWF19L1):c.1065A>G (p.Lys355=)	CWF19L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 730375	NM_018294.6(CWF19L1):c.940C>T (p.His314Tyr)	CWF19L1 (H314Y +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive spinocerebellar ataxia 17 +1 more	GBenign
Select item 722957	NM_018294.6(CWF19L1):c.965-6A>G	CWF19L1	Single nucleotide variant (intron variant)	not provided	GBenign/Likely benign
Select item 719079	NM_018294.6(CWF19L1):c.375T>C (p.Gly125=)	CWF19L1	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 716214	NM_018294.6(CWF19L1):c.257G>A (p.Gly86Glu)	CWF19L1 (G86E)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 716213	NM_018294.6(CWF19L1):c.1395A>C (p.Ala465=)	CWF19L1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 715239	NM_018294.6(CWF19L1):c.1419A>C (p.Thr473=)	CWF19L1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 708368	NM_018294.6(CWF19L1):c.1511A>T (p.Asp504Val)	CHUK-DT, CWF19L1 (D259V +3 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 563802	GRCh37/hg19 10q23.33-26.3(chr10:94346520-135427143)x3	ABCC2, ABLIM1 +298 more	Copy number gain	not provided	GPathogenic
Select item 523165	GRCh37/hg19 10q11.21-26.3(chr10:42347406-135534747)x1	COX15, CPEB3 +569 more	Copy number loss	Poly (ADP-Ribose) polymerase inhibitor response	Gdrug response
Select item 504148	NM_018294.6(CWF19L1):c.1466_1467del (p.Phe489fs)	CWF19L1 (F489fs +3 more)	Deletion (frameshift variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 504028	NM_018294.6(CWF19L1):c.779del (p.Asp260fs)	CWF19L1 (D123fs +2 more)	Deletion (frameshift variant)	not provided	GPathogenic

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