ClinVar Miner

List of variants reported as uncertain significance for Herpesviridae infectious disease

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 109
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HGVS dbSNP
NC_000004.11:g.(?_186997754)_(187006047_?)dup
NC_000011.9:g.(?_67758997)_(67759348_?)dup
NC_000011.9:g.(?_67758997)_(67761285_?)dup
NC_000014.8:g.(?_103336519)_(103397037_?)dup
NC_000014.8:g.(?_103355877)_(103395332_?)dup
NM_003265.2(TLR3):c.1072G>A (p.Glu358Lys)
NM_003265.2(TLR3):c.1234C>G (p.Leu412Val)
NM_003265.2(TLR3):c.1378G>A (p.Glu460Lys)
NM_003265.2(TLR3):c.1430C>T (p.Ala477Val)
NM_003265.2(TLR3):c.1471G>A (p.Ala491Thr)
NM_003265.2(TLR3):c.1489A>G (p.Ser497Gly) rs369886993
NM_003265.2(TLR3):c.1559A>G (p.Asn520Ser)
NM_003265.2(TLR3):c.1660C>T (p.Pro554Ser) rs121434431
NM_003265.2(TLR3):c.176C>A (p.Thr59Asn)
NM_003265.2(TLR3):c.1774G>A (p.Asp592Asn)
NM_003265.2(TLR3):c.1854del (p.Lys619fs) rs1561372514
NM_003265.2(TLR3):c.1928G>A (p.Arg643His)
NM_003265.2(TLR3):c.205G>A (p.Ala69Thr)
NM_003265.2(TLR3):c.2228G>A (p.Gly743Asp) rs1280549921
NM_003265.2(TLR3):c.2265A>G (p.Glu755=) rs1554064947
NM_003265.2(TLR3):c.2371A>G (p.Arg791Gly)
NM_003265.2(TLR3):c.2384C>T (p.Ala795Val)
NM_003265.2(TLR3):c.2497C>T (p.His833Tyr) rs1460329308
NM_003265.2(TLR3):c.2654G>A (p.Arg885Gln)
NM_003265.2(TLR3):c.266A>C (p.Lys89Thr)
NM_003265.2(TLR3):c.2693G>A (p.Gly898Glu)
NM_003265.2(TLR3):c.442-6C>G
NM_003265.2(TLR3):c.554C>T (p.Ala185Val)
NM_003265.2(TLR3):c.585del (p.Asn196fs)
NM_003265.2(TLR3):c.655G>A (p.Ala219Thr)
NM_003265.2(TLR3):c.71C>T (p.Ser24Phe)
NM_003265.2(TLR3):c.889C>G (p.Leu297Val) rs35311343
NM_003265.2(TLR3):c.958G>A (p.Gly320Arg) rs554658931
NM_030930.4(UNC93B1):c.1121G>A (p.Arg374Gln)
NM_030930.4(UNC93B1):c.1138G>A (p.Val380Met)
NM_030930.4(UNC93B1):c.1210C>T (p.Pro404Ser) rs377021545
NM_030930.4(UNC93B1):c.1303C>A (p.Leu435Ile)
NM_030930.4(UNC93B1):c.1482+2T>A
NM_030930.4(UNC93B1):c.1594C>A (p.Pro532Thr) rs543443741
NM_030930.4(UNC93B1):c.1657G>A (p.Glu553Lys)
NM_030930.4(UNC93B1):c.1661G>A (p.Gly554Asp) rs2375179
NM_030930.4(UNC93B1):c.1703G>A (p.Gly568Glu)
NM_030930.4(UNC93B1):c.1720G>C (p.Glu574Gln)
NM_030930.4(UNC93B1):c.1726G>C (p.Ala576Pro)
NM_030930.4(UNC93B1):c.1735G>C (p.Gly579Arg)
NM_030930.4(UNC93B1):c.1768G>A (p.Gly590Arg)
NM_030930.4(UNC93B1):c.1792T>G (p.Ter598Gly)
NM_030930.4(UNC93B1):c.190G>A (p.Val64Met)
NM_030930.4(UNC93B1):c.193C>G (p.Leu65Val)
NM_030930.4(UNC93B1):c.409T>C (p.Trp137Arg) rs1554985993
NM_030930.4(UNC93B1):c.424G>A (p.Ala142Thr)
NM_030930.4(UNC93B1):c.491C>T (p.Ser164Leu)
NM_030930.4(UNC93B1):c.586T>C (p.Tyr196His)
NM_030930.4(UNC93B1):c.618G>T (p.Gln206His) rs1435279681
NM_030930.4(UNC93B1):c.654G>A (p.Leu218=)
NM_030930.4(UNC93B1):c.667A>G (p.Ile223Val)
NM_030930.4(UNC93B1):c.748C>A (p.Leu250Met)
NM_030930.4(UNC93B1):c.818A>G (p.Lys273Arg)
NM_030930.4(UNC93B1):c.923G>C (p.Gly308Ala) rs1442000007
NM_030930.4(UNC93B1):c.958C>T (p.Arg320Cys) rs1565124797
NM_030930.4(UNC93B1):c.998A>G (p.Lys333Arg)
NM_145725.2(TRAF3):c.1021C>T (p.Arg341Trp)
NM_145725.2(TRAF3):c.1109G>A (p.Ser370Asn)
NM_145725.2(TRAF3):c.1200C>A (p.Ala400=)
NM_145725.2(TRAF3):c.1425dup (p.Val476fs)
NM_145725.2(TRAF3):c.199G>A (p.Glu67Lys) rs1566786155
NM_145725.2(TRAF3):c.297+6del
NM_145725.2(TRAF3):c.487C>T (p.Arg163Ter) rs1566789877
NM_145725.2(TRAF3):c.488G>A (p.Arg163Gln)
NM_145725.2(TRAF3):c.676G>T (p.Val226Phe) rs1384888729
NM_145725.2(TRAF3):c.735C>A (p.Asn245Lys)
NM_145725.2(TRAF3):c.806C>T (p.Ser269Leu)
NM_145725.2(TRAF3):c.856_857del (p.Lys286fs) rs1555376796
NM_145725.2(TRAF3):c.962G>A (p.Arg321Gln)
NM_182919.3(TICAM1):c.1054A>C (p.Thr352Pro)
NM_182919.3(TICAM1):c.1078_1080CCT[10] (p.Pro366_Pro367dup) rs11466722
NM_182919.3(TICAM1):c.1130C>A (p.Thr377Asn)
NM_182919.3(TICAM1):c.1216G>A (p.Glu406Lys)
NM_182919.3(TICAM1):c.1264C>T (p.Pro422Ser) rs140568066
NM_182919.3(TICAM1):c.1388G>A (p.Arg463His) rs1555730200
NM_182919.3(TICAM1):c.1556T>A (p.Ile519Asn) rs772590478
NM_182919.3(TICAM1):c.1632G>C (p.Gln544His)
NM_182919.3(TICAM1):c.1669G>A (p.Asp557Asn) rs143066432
NM_182919.3(TICAM1):c.1720C>G (p.Leu574Val)
NM_182919.3(TICAM1):c.1774G>A (p.Gly592Arg)
NM_182919.3(TICAM1):c.1882C>T (p.Pro628Ser)
NM_182919.3(TICAM1):c.197C>T (p.Ala66Val) rs1437926927
NM_182919.3(TICAM1):c.2107G>A (p.Ala703Thr)
NM_182919.3(TICAM1):c.212G>A (p.Arg71Gln)
NM_182919.3(TICAM1):c.238G>A (p.Val80Met) rs199816697
NM_182919.3(TICAM1):c.269C>A (p.Pro90Gln) rs141687483
NM_182919.3(TICAM1):c.331G>A (p.Ala111Thr)
NM_182919.3(TICAM1):c.346G>A (p.Val116Met)
NM_182919.3(TICAM1):c.364G>A (p.Val122Ile)
NM_182919.3(TICAM1):c.395G>A (p.Arg132Gln)
NM_182919.3(TICAM1):c.434G>T (p.Gly145Val)
NM_182919.3(TICAM1):c.443T>C (p.Ile148Thr) rs1202936308
NM_182919.3(TICAM1):c.446C>G (p.Ala149Gly)
NM_182919.3(TICAM1):c.470C>T (p.Thr157Met)
NM_182919.3(TICAM1):c.538C>T (p.Arg180Cys) rs141394423
NM_182919.3(TICAM1):c.557C>T (p.Ser186Leu) rs146550489
NM_182919.3(TICAM1):c.614G>A (p.Ser205Asn) rs754876060
NM_182919.3(TICAM1):c.697G>A (p.Asp233Asn)
NM_182919.3(TICAM1):c.697G>C (p.Asp233His)
NM_182919.3(TICAM1):c.718C>T (p.Pro240Ser)
NM_182919.3(TICAM1):c.721G>A (p.Glu241Lys)
NM_182919.3(TICAM1):c.7T>G (p.Cys3Gly)
NM_182919.3(TICAM1):c.826C>T (p.Pro276Ser)
NM_182919.3(TICAM1):c.935A>G (p.Gln312Arg)

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