ClinVar Miner

List of variants in gene VIPAS39 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_001193315.2(VIPAS39):c.196+55A>G rs2364158 0.95342
NM_001193315.2(VIPAS39):c.196+224A>G rs2364157 0.95335
NM_001193315.2(VIPAS39):c.913-172G>T rs1008669 0.95259
NM_001193315.2(VIPAS39):c.1356+230A>G rs2242619 0.42634
NM_001193315.2(VIPAS39):c.734+315T>C rs11625365 0.41459
NM_001193315.2(VIPAS39):c.504+85T>C rs2091916 0.41429
NM_001193315.2(VIPAS39):c.1047+146G>T rs963283 0.41411
NM_001193315.2(VIPAS39):c.837-156T>C rs2063997 0.28254
NM_001193315.2(VIPAS39):c.343+118T>C rs11159260 0.17462
NM_001193315.2(VIPAS39):c.504+163A>G rs10483882 0.16751
NM_001193315.2(VIPAS39):c.197-192T>G rs56235462 0.16272
NM_001193315.2(VIPAS39):c.1089+115A>C rs67370165 0.15774
NM_001193315.2(VIPAS39):c.344-110A>G rs760252 0.15413
NM_001193315.2(VIPAS39):c.1179+20G>A rs34835605 0.15384
NM_001193315.2(VIPAS39):c.598-278G>A rs12885247 0.14541
NM_001193315.2(VIPAS39):c.1267-200C>A rs11624682 0.04151
NM_001193315.2(VIPAS39):c.234C>T (p.Ser78=) rs17105802 0.03528
NM_001193315.2(VIPAS39):c.343+98G>A rs17105800 0.03285
NM_001193315.2(VIPAS39):c.448-56T>C rs75957729 0.03281
NM_001193315.2(VIPAS39):c.1180-177T>C rs78774970 0.03280
NM_001193315.2(VIPAS39):c.448-105T>G rs79727874 0.03278
NM_001193315.2(VIPAS39):c.196+220T>G rs76221293 0.03277
NM_001193315.2(VIPAS39):c.344-90T>A rs17105799 0.03277
NM_001193315.2(VIPAS39):c.94-46G>T rs76683141 0.03256
NM_001193315.2(VIPAS39):c.735-45A>G rs76396354 0.03203
NM_001193315.2(VIPAS39):c.598-55A>G rs112864545 0.03200
NM_001193315.2(VIPAS39):c.836+201A>G rs77989129 0.03195
NM_001193315.2(VIPAS39):c.912+149C>T rs79242802 0.03178
NM_001193315.2(VIPAS39):c.1266+216_1266+217insGAGAGCTGTG rs376721563 0.03166
NM_001193315.2(VIPAS39):c.1266+220_1266+221insG rs201469802 0.03166
NM_001193315.2(VIPAS39):c.1266+218del rs1199506236 0.03164
NM_001193315.2(VIPAS39):c.504+116A>T rs76597851 0.02959
NM_001193315.2(VIPAS39):c.1356+212C>T rs77502922 0.02079
NM_001193315.2(VIPAS39):c.734+149T>G rs55665986 0.01885
NM_001193315.2(VIPAS39):c.1179+13C>G rs146288421 0.00742
NM_001193315.2(VIPAS39):c.836+15A>G rs142958086 0.00739
NM_001193315.2(VIPAS39):c.1242G>A (p.Leu414=) rs45447095 0.00453
NM_001193315.2(VIPAS39):c.861C>T (p.Ser287=) rs148698913 0.00275
NM_001193315.2(VIPAS39):c.632-14T>C rs142501624 0.00164
NM_001193315.2(VIPAS39):c.1450C>T (p.Leu484Phe) rs75211061 0.00142
NM_001193315.2(VIPAS39):c.1455C>A (p.Ser485Arg) rs145453157 0.00129
NM_001193315.2(VIPAS39):c.136G>A (p.Val46Met) rs148360332 0.00106
NM_001193315.2(VIPAS39):c.972C>T (p.Arg324=) rs147303718 0.00084
NM_001193315.2(VIPAS39):c.598-6C>G rs141155709 0.00081
NM_001193315.2(VIPAS39):c.1065C>T (p.Pro355=) rs118155418 0.00042
NM_001193315.2(VIPAS39):c.1254T>C (p.Asn418=) rs188105111 0.00008
NM_001193315.2(VIPAS39):c.1014C>T (p.Phe338=) rs199839422 0.00001
NM_001193315.2(VIPAS39):c.1180-16del
NM_001193315.2(VIPAS39):c.383-74C>G rs76742098
NM_001193315.2(VIPAS39):c.447+14T>C
NM_001193315.2(VIPAS39):c.597+193_597+195dup rs35983631
NM_001193315.2(VIPAS39):c.597+193dup rs35983631
NM_001193315.2(VIPAS39):c.631+125_631+139del rs146236367
NM_001193315.2(VIPAS39):c.632-13G>A
NM_001193315.2(VIPAS39):c.735-280del rs34716621
NM_001193315.2(VIPAS39):c.762+177dup rs11388351
NM_001193315.2(VIPAS39):c.912+20T>C
NM_001193315.2(VIPAS39):c.913-12A>G
NM_001193315.2(VIPAS39):c.913-36_913-33dup rs3075829
NM_001193315.2(VIPAS39):c.913-36_913-34dup rs3075829
NM_001193315.2(VIPAS39):c.913-36_913-35dup rs3075829
NM_001193315.2(VIPAS39):c.913-36dup rs3075829

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