List of variants in gene VCL reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 100

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HGVS	dbSNP	gnomAD frequency
NM_014000.3(VCL):c.*1854A>C	rs3829204	0.11656
NM_014000.3(VCL):c.768T>C (p.Asp256=)	rs56413529	0.06776
NM_014000.3(VCL):c.339G>A (p.Arg113=)	rs56314318	0.06767
NM_014000.3(VCL):c.*1853A>C	rs554923257	0.04999
NM_014000.3(VCL):c.1557C>A (p.Ile519=)	rs150120464	0.00466
NM_014000.3(VCL):c.2434+19T>C	rs188216596	0.00198
NM_014000.3(VCL):c.1353-19G>A	rs145537824	0.00193
NM_014000.3(VCL):c.*646C>G	rs41280414	0.00112
NM_014000.3(VCL):c.1572C>T (p.Ala524=)	rs138566234	0.00086
NM_014000.3(VCL):c.1348A>C (p.Arg450=)	rs142128712	0.00075
NM_014000.3(VCL):c.*1282C>T	rs529687198	0.00054
NM_014000.3(VCL):c.1237G>A (p.Ala413Thr)	rs146278697	0.00044
NM_014000.3(VCL):c.*1659C>T	rs1804893	0.00040
NM_014000.3(VCL):c.1626C>T (p.Leu542=)	rs150402791	0.00031
NM_014000.3(VCL):c.*1285C>T	rs879813349	0.00027
NM_014000.3(VCL):c.787A>T (p.Thr263Ser)	rs142233726	0.00022
NM_014000.3(VCL):c.2969C>T (p.Ala990Val)	rs150595117	0.00019
NM_014000.3(VCL):c.*212C>A	rs757322860	0.00012
NM_014000.3(VCL):c.*1761A>G	rs886047230	0.00010
NM_014000.3(VCL):c.688C>T (p.Arg230Cys)	rs139312390	0.00010
NM_014000.3(VCL):c.829C>A (p.Leu277Met)	rs71579353	0.00010
NM_014000.3(VCL):c.1490T>C (p.Ile497Thr)	rs572757800	0.00008
NM_014000.3(VCL):c.1621C>G (p.Leu541Val)	rs370229150	0.00008
NM_014000.3(VCL):c.2444A>G (p.Lys815Arg)	rs373010557	0.00008
NM_014000.3(VCL):c.1195A>C (p.Asn399His)	rs377228795	0.00006
NM_014000.3(VCL):c.2468G>A (p.Arg823Gln)	rs759202535	0.00006
NM_014000.3(VCL):c.2531C>T (p.Pro844Leu)	rs145393322	0.00006
NM_014000.3(VCL):c.2649A>C (p.Glu883Asp)	rs752902180	0.00006
NM_014000.3(VCL):c.592G>A (p.Val198Met)	rs760340545	0.00006
NM_014000.3(VCL):c.1287T>A (p.Asp429Glu)	rs139371702	0.00005
NM_014000.3(VCL):c.1583G>A (p.Arg528His)	rs746095066	0.00005
NM_014000.3(VCL):c.1192C>T (p.Pro398Ser)	rs201528612	0.00004
NM_014000.3(VCL):c.1511T>C (p.Ile504Thr)	rs745343813	0.00004
NM_014000.3(VCL):c.1928C>T (p.Thr643Met)	rs150643310	0.00004
NM_014000.3(VCL):c.2046A>T (p.Leu682Phe)	rs565398652	0.00004
NM_014000.3(VCL):c.2399A>T (p.Asp800Val)	rs919509789	0.00004
NM_014000.3(VCL):c.3092G>A (p.Arg1031Gln)	rs397517238	0.00004
NM_014000.3(VCL):c.1039C>T (p.Pro347Ser)	rs566961713	0.00003
NM_014000.3(VCL):c.1040C>T (p.Pro347Leu)	rs148619523	0.00003
NM_014000.3(VCL):c.1940C>T (p.Ala647Val)	rs534449109	0.00003
NM_014000.3(VCL):c.2443A>G (p.Lys815Glu)	rs960017518	0.00003
NM_014000.3(VCL):c.1031G>C (p.Gly344Ala)	rs778875353	0.00002
NM_014000.3(VCL):c.1558C>T (p.Arg520Trp)	rs377722209	0.00002
NM_014000.3(VCL):c.1606C>A (p.Pro536Thr)	rs370058111	0.00002
NM_014000.3(VCL):c.2038C>T (p.Arg680Cys)	rs759356162	0.00002
NM_014000.3(VCL):c.2747C>T (p.Pro916Leu)	rs143321584	0.00002
NM_014000.3(VCL):c.2905G>A (p.Ala969Thr)	rs199751261	0.00002
NM_014000.3(VCL):c.806C>G (p.Ala269Gly)	rs762710405	0.00002
NM_014000.3(VCL):c.853C>T (p.Arg285Cys)	rs757517552	0.00002
NM_014000.3(VCL):c.1046C>T (p.Ala349Val)	rs777709634	0.00001
NM_014000.3(VCL):c.1246C>T (p.Arg416Trp)	rs746004026	0.00001
NM_014000.3(VCL):c.1298G>A (p.Arg433His)	rs754046223	0.00001
NM_014000.3(VCL):c.1435C>T (p.Arg479Trp)	rs369055603	0.00001
NM_014000.3(VCL):c.1465G>A (p.Ala489Thr)	rs1449290312	0.00001
NM_014000.3(VCL):c.1503G>C (p.Gln501His)	rs1203105475	0.00001
NM_014000.3(VCL):c.1640G>A (p.Arg547Gln)	rs748044427	0.00001
NM_014000.3(VCL):c.1865G>A (p.Arg622Lys)	rs771590749	0.00001
NM_014000.3(VCL):c.2001G>A (p.Thr667=)	rs747424067	0.00001
NM_014000.3(VCL):c.2023-1G>C	rs1840093670	0.00001
NM_014000.3(VCL):c.2285G>A (p.Arg762Gln)	rs540039788	0.00001
NM_014000.3(VCL):c.2305A>G (p.Arg769Gly)	rs566257885	0.00001
NM_014000.3(VCL):c.238A>C (p.Lys80Gln)	rs775532257	0.00001
NM_014000.3(VCL):c.239+11G>A	rs918332199	0.00001
NM_014000.3(VCL):c.239+6T>G	rs752335603	0.00001
NM_014000.3(VCL):c.2528C>T (p.Pro843Leu)	rs764302249	0.00001
NM_014000.3(VCL):c.2558G>A (p.Arg853Gln)	rs992716111	0.00001
NM_014000.3(VCL):c.2807C>T (p.Ala936Val)	rs754681045	0.00001
NM_014000.3(VCL):c.2893C>T (p.Pro965Ser)	rs749236817	0.00001
NM_014000.3(VCL):c.2923C>T (p.Arg975Trp)	rs121917776	0.00001
NM_014000.3(VCL):c.2924G>A (p.Arg975Gln)	rs767325003	0.00001
NM_014000.3(VCL):c.313C>T (p.Arg105Ter)	rs397517239	0.00001
NM_014000.3(VCL):c.3381T>C (p.Val1127=)	rs943734765	0.00001
NM_014000.3(VCL):c.527A>G (p.Asp176Gly)	rs573623641	0.00001
NM_014000.3(VCL):c.550C>T (p.His184Tyr)	rs1321660809	0.00001
NM_014000.3(VCL):c.739G>A (p.Val247Met)	rs545372383	0.00001
NM_014000.3(VCL):c.844G>T (p.Gly282Cys)	rs766091503	0.00001
NM_014000.3(VCL):c.952C>T (p.Arg318Cys)	rs397517247	0.00001
NM_014000.3(VCL):c.*1794G>A	rs577038840
NM_014000.3(VCL):c.1132A>G (p.Thr378Ala)	rs2131907756
NM_014000.3(VCL):c.1225C>G (p.Arg409Gly)	rs202005455
NM_014000.3(VCL):c.1296_1297inv (p.Arg433Cys)
NM_014000.3(VCL):c.1354G>A (p.Gly452Arg)	rs1015527957
NM_014000.3(VCL):c.1457C>T (p.Pro486Leu)	rs1251509217
NM_014000.3(VCL):c.1620T>A (p.Asp540Glu)	rs533622785
NM_014000.3(VCL):c.169-11del	rs753900484
NM_014000.3(VCL):c.1743+6A>G	rs370709860
NM_014000.3(VCL):c.1744-1G>T	rs1057524654
NM_014000.3(VCL):c.1819A>C (p.Lys607Gln)	rs794729192
NM_014000.3(VCL):c.1879G>A (p.Asp627Asn)	rs1251173111
NM_014000.3(VCL):c.2022+5G>T	rs1050797785
NM_014000.3(VCL):c.2407G>A (p.Ala803Thr)	rs754294941
NM_014000.3(VCL):c.2579del (p.Pro860fs)	rs1840179829
NM_014000.3(VCL):c.2775_2780del (p.Gly926_Val927del)	rs757018106
NM_014000.3(VCL):c.2823_2824delinsGT (p.Pro942Ser)	rs1060502196
NM_014000.3(VCL):c.2866A>G (p.Met956Val)	rs761830073
NM_014000.3(VCL):c.482C>G (p.Thr161Arg)	rs376226543
NM_014000.3(VCL):c.565G>T (p.Val189Leu)	rs151045204
NM_014000.3(VCL):c.625A>G (p.Met209Val)	rs144683137
NM_014000.3(VCL):c.686dup (p.Asn229fs)	rs776583302
NM_014000.3(VCL):c.768T>A (p.Asp256Glu)	rs56413529

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