ClinVar Miner

List of variants in gene F5 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 124
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HGVS dbSNP gnomAD frequency
NM_000130.5(F5):c.1601= (p.Arg534=) rs6025 0.98238
NM_000130.5(F5):c.1296+242C>T rs2213868 0.95218
NM_000130.5(F5):c.4972-330G>T rs6427197 0.92388
NM_000130.5(F5):c.1763-260T>C rs1018827 0.92090
NM_000130.5(F5):c.587-296G>A rs6427202 0.67588
NM_000130.5(F5):c.731-320C>A rs4656188 0.59853
NM_000130.5(F5):c.731-195G>A rs4656688 0.59845
NM_000130.5(F5):c.731-262T>C rs4656689 0.59834
NM_000130.5(F5):c.952+118A>G rs2239853 0.59808
NM_000130.5(F5):c.1297-121T>C rs10800456 0.43043
NM_000130.5(F5):c.5788+122T>G rs12131397 0.41947
NM_000130.5(F5):c.1397-164C>T rs7537742 0.41696
NM_000130.5(F5):c.1976-291T>G rs6686805 0.41489
NM_000130.5(F5):c.5717-50G>A rs2301515 0.38964
NM_000130.5(F5):c.5209-134T>C rs2157581 0.38597
NM_000130.5(F5):c.1976-172G>A rs2239852 0.38298
NM_000130.5(F5):c.3804T>C (p.Ser1268=) rs1800594 0.33303
NM_000130.5(F5):c.374-89A>G rs7534848 0.33170
NM_000130.5(F5):c.374-66T>G rs7545236 0.33152
NM_000130.5(F5):c.1397-296C>T rs1988608 0.33020
NM_000130.5(F5):c.587-46G>A rs6012 0.32719
NM_000130.5(F5):c.374-172G>C rs7522982 0.32713
NM_000130.5(F5):c.587-188G>A rs6427201 0.32696
NM_000130.5(F5):c.1611+264T>C rs10800455 0.32084
NM_000130.5(F5):c.1296+244G>C rs721161 0.31934
NM_000130.5(F5):c.6528+130A>C rs3820060 0.31625
NC_000001.11:g.169586812C>T rs2269648 0.30179
NM_000130.5(F5):c.4095C>T (p.Thr1365=) rs9332607 0.29522
NM_000130.5(F5):c.5290A>G (p.Met1764Val) rs6030 0.29437
NM_000130.5(F5):c.952+76C>T rs2239854 0.27986
NM_000130.5(F5):c.6529-147G>A rs4656685 0.25339
NM_000130.5(F5):c.*1601C>T rs2187952 0.25334
NM_000130.5(F5):c.5600-178A>G rs9332635 0.24222
NM_000130.5(F5):c.5893-86G>A rs9332643 0.24200
NM_000130.5(F5):c.4972-88C>T rs9332619 0.24167
NM_000130.5(F5):c.2573A>G (p.Lys858Arg) rs4524 0.24159
NM_000130.5(F5):c.5208+73G>A rs9332620 0.24159
NM_000130.5(F5):c.1976-145G>T rs2239851 0.24153
NM_000130.5(F5):c.1976-299C>T rs6662696 0.24152
NM_000130.5(F5):c.2208C>T (p.Ile736=) rs6016 0.24147
NM_000130.5(F5):c.1976-210A>G rs6675244 0.24144
NM_000130.5(F5):c.2594A>G (p.His865Arg) rs4525 0.24141
NM_000130.5(F5):c.2301A>G (p.Ser767=) rs6021 0.24140
NM_000130.5(F5):c.2773A>G (p.Lys925Glu) rs6032 0.24133
NM_000130.5(F5):c.6193+246T>C rs2213866 0.24080
NM_000130.5(F5):c.6193+173A>G rs2213867 0.24065
NM_000130.5(F5):c.1976-242C>T rs6662593 0.23925
NM_000130.5(F5):c.2235T>C (p.Asn745=) rs6017 0.23336
NM_000130.5(F5):c.1612-44A>T rs13306345 0.23267
NM_000130.5(F5):c.1612-106A>G rs79186925 0.23235
NM_000130.5(F5):c.1975+98G>T rs9287092 0.23009
NM_000130.5(F5):c.1762+144G>A rs6672595 0.22997
NM_000130.5(F5):c.237A>G (p.Gln79=) rs6028 0.22486
NM_000130.5(F5):c.3948C>T (p.Leu1316=) rs9287090 0.21875
NM_000130.5(F5):c.1612-86C>T rs13306344 0.20457
NM_000130.5(F5):c.3853C>A (p.Leu1285Ile) rs1046712 0.16155
NM_000130.5(F5):c.319G>C (p.Asp107His) rs6019 0.14054
NM_000130.5(F5):c.374-73C>A rs7523043 0.13918
NM_000130.5(F5):c.1538G>A (p.Arg513Lys) rs6020 0.11893
NM_000130.5(F5):c.1396+113T>C rs13306331 0.09825
NM_000130.5(F5):c.1396+207A>G rs59548259 0.08999
NM_000130.5(F5):c.1612-95T>C rs12139696 0.08898
NM_000130.5(F5):c.4972-221C>T rs9332618 0.08804
NM_000130.5(F5):c.1242A>G (p.Lys414=) rs6035 0.08632
NM_000130.5(F5):c.953-255C>T rs57637273 0.08201
NM_000130.5(F5):c.5717-257A>G rs2301517 0.07753
NM_000130.5(F5):c.1380C>T (p.Asn460=) rs6015 0.06377
NM_000130.5(F5):c.1716G>A (p.Glu572=) rs6036 0.06356
NM_000130.5(F5):c.1238T>C (p.Met413Thr) rs6033 0.06350
NM_000130.5(F5):c.1926C>A (p.Thr642=) rs6037 0.06314
NM_000130.5(F5):c.730+7C>T rs6023 0.05754
NM_000130.5(F5):c.*1820A>C rs72708013 0.05470
NM_000130.5(F5):c.*873C>T rs9332673 0.05461
NM_000130.5(F5):c.2450A>C (p.Asn817Thr) rs6018 0.05391
NM_000130.5(F5):c.2289A>G (p.Glu763=) rs6024 0.05387
NM_000130.5(F5):c.4796+49A>C rs9332609 0.05384
NM_000130.5(F5):c.6665A>G (p.Asp2222Gly) rs6027 0.05290
NM_000130.5(F5):c.5788+180T>C rs9332639 0.05284
NM_000130.5(F5):c.3980A>G (p.His1327Arg) rs1800595 0.05074
NM_000130.5(F5):c.730+211G>T rs9332569 0.04928
NM_000130.5(F5):c.5022A>G (p.Gly1674=) rs6010 0.04908
NM_000130.5(F5):c.158+237A>G rs9332486 0.04892
NM_000130.5(F5):c.4210C>T (p.Pro1404Ser) rs9332608 0.04654
NM_000130.5(F5):c.6049-44T>C rs9332658 0.04504
NM_000130.5(F5):c.4189C>T (p.Leu1397Phe) rs13306334 0.03498
NM_000130.5(F5):c.586+37T>C rs2157583 0.03449
NM_000130.5(F5):c.159-106G>A rs60781559 0.03254
NM_000130.5(F5):c.251-259C>T rs9332524 0.03252
NC_000001.11:g.169586807C>G rs9332483 0.03249
NM_000130.5(F5):c.250+229C>T rs9332498 0.03240
NM_000130.5(F5):c.2425C>T (p.Pro809Ser) rs6031 0.02430
NM_000130.5(F5):c.1397-51T>C rs9332693 0.01836
NC_000001.11:g.169586581C>T rs9332484 0.01699
NM_000130.5(F5):c.3845A>G (p.His1282Arg) rs143333036 0.00389
NM_000130.5(F5):c.2129A>G (p.His710Arg) rs115954845 0.00366
NM_000130.5(F5):c.6554A>G (p.Lys2185Arg) rs6679078 0.00271
NC_000001.11:g.169586735G>C rs16862404
NM_000130.5(F5):c.*1436T>A rs9332678
NM_000130.5(F5):c.1296+62G>A rs9332582
NM_000130.5(F5):c.1397-255A>G rs1988607
NM_000130.5(F5):c.158+87dup rs372224504
NM_000130.5(F5):c.1611+154dup rs55717622
NM_000130.5(F5):c.1611+166del rs55717622
NM_000130.5(F5):c.1611+218_1611+219del rs56100784
NM_000130.5(F5):c.1612-309C>G rs12143223
NM_000130.5(F5):c.1762+233_1762+234insAT rs112177003
NM_000130.5(F5):c.1762+234GT[12] rs3835453
NM_000130.5(F5):c.1762+234GT[13] rs3835453
NM_000130.5(F5):c.1762+234GT[15] rs3835453
NM_000130.5(F5):c.1762+299A>G rs1894694
NM_000130.5(F5):c.250+104G>A rs113027984
NM_000130.5(F5):c.250+110_250+111dup rs56901113
NM_000130.5(F5):c.250+110dup rs56901113
NM_000130.5(F5):c.4971+186del rs58033656
NM_000130.5(F5):c.5419+11C>T rs6008
NM_000130.5(F5):c.564G>C (p.Gly188=) rs1557573
NM_000130.5(F5):c.6048+181_6048+184del rs79717313
NM_000130.5(F5):c.6194-20C>A rs6013
NM_000130.5(F5):c.6529-65A>C rs2227243
NM_000130.5(F5):c.730+137_730+139dup rs58738850
NM_000130.5(F5):c.730+137_730+140dup rs58738850
NM_000130.5(F5):c.730+316G>C rs9332570
NM_000130.5(F5):c.731-160dup rs9332577
NM_000130.5(F5):c.952+326_952+327insGCCAGAG rs16684

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