ClinVar Miner

List of variants reported as benign for Herpes simplex encephalitis, susceptibility to, 1

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_030930.4(UNC93B1):c.1557C>G (p.Arg519=) rs7149 0.33574
NM_003265.3(TLR3):c.1377C>T (p.Phe459=) rs3775290 0.27464
NM_003265.3(TLR3):c.-7C>A rs3775296 0.17880
NM_003265.3(TLR3):c.2553C>T (p.Phe851=) rs73873710 0.05231
NM_003265.3(TLR3):c.1704C>T (p.Asn568=) rs35111588 0.04959
NM_030930.4(UNC93B1):c.1206G>C (p.Pro402=) rs112284414 0.02672
NM_003265.3(TLR3):c.1677G>A (p.Lys559=) rs35617964 0.01248
NM_030930.4(UNC93B1):c.1163C>T (p.Ala388Val) rs11543208 0.01149
NM_003265.3(TLR3):c.919T>G (p.Tyr307Asp) rs5743317 0.01113
NM_003265.3(TLR3):c.2209T>A (p.Ser737Thr) rs5743318 0.01027
NM_003265.3(TLR3):c.1927C>A (p.Arg643Ser) rs73025939 0.00959
NM_030930.4(UNC93B1):c.1155C>T (p.Gly385=) rs200930438 0.00789
NM_003265.3(TLR3):c.838G>A (p.Asp280Asn) rs112077022 0.00550
NM_003265.3(TLR3):c.2556T>G (p.Leu852=) rs115677523 0.00545
NM_030930.4(UNC93B1):c.1725C>G (p.Pro575=) rs568350079 0.00509
NM_030930.4(UNC93B1):c.1772G>A (p.Gly591Glu) rs531159136 0.00330
NM_030930.4(UNC93B1):c.907-5C>T rs144979304 0.00312
NM_030930.4(UNC93B1):c.393-10C>T rs117183629 0.00307
NM_030930.4(UNC93B1):c.626C>T (p.Pro209Leu) rs144399212 0.00265
NM_030930.4(UNC93B1):c.385C>A (p.Leu129Ile) rs146593182 0.00262
NM_030930.4(UNC93B1):c.1453G>A (p.Val485Met) rs199824078 0.00237
NM_003265.3(TLR3):c.634-10C>A rs113654222 0.00229
NM_030930.4(UNC93B1):c.97-8G>T rs539458551 0.00220
NM_003265.3(TLR3):c.727T>C (p.Leu243=) rs75290011 0.00187
NM_003265.3(TLR3):c.612G>A (p.Leu204=) rs5743311 0.00180
NM_030930.4(UNC93B1):c.239-6C>T rs182093266 0.00177
NM_003265.3(TLR3):c.2224C>T (p.Leu742Phe) rs147431766 0.00153
NM_003265.3(TLR3):c.2664C>T (p.Ala888=) rs5743320 0.00143
NM_030930.4(UNC93B1):c.1713T>C (p.Pro571=) rs565846179 0.00106
NM_003265.3(TLR3):c.2217T>C (p.His739=) rs116269970 0.00096
NM_030930.4(UNC93B1):c.96+10G>A rs188940236 0.00090
NM_003265.3(TLR3):c.1284T>G (p.Ser428=) rs148445556 0.00073
NM_030930.4(UNC93B1):c.1449C>T (p.Phe483=) rs371738908 0.00019
NM_030930.4(UNC93B1):c.1183C>T (p.Leu395=) rs776764518 0.00017
NM_003265.3(TLR3):c.1683G>A (p.Leu561=) rs571300094 0.00002
NM_003265.3(TLR3):c.1234C>T (p.Leu412Phe) rs3775291
NM_003265.3(TLR3):c.2487-7dup rs779960687
NM_003265.3(TLR3):c.634-12del rs746858510
NM_030930.4(UNC93B1):c.1090-10dup rs760132599
NM_030930.4(UNC93B1):c.1221C>T (p.Ala407=) rs12660
NM_030930.4(UNC93B1):c.1495G>A (p.Val499Met) rs4014596
NM_030930.4(UNC93B1):c.1724_1725delinsAG (p.Pro575Gln) rs1554984685
NM_030930.4(UNC93B1):c.1768G>T (p.Gly590Trp) rs2375182
NM_030930.4(UNC93B1):c.888dup (p.Phe297fs) rs5792426

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