ClinVar Miner

List of variants reported as likely benign for Herpesviridae infectious disease by Invitae

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 33
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HGVS dbSNP
NM_003265.2(TLR3):c.165G>A (p.Val55=) rs139854420
NM_003265.2(TLR3):c.1716C>T (p.Asn572=) rs140712645
NM_003265.2(TLR3):c.1834C>T (p.Leu612=) rs781622881
NM_003265.2(TLR3):c.2011C>T (p.Leu671=) rs144019953
NM_003265.2(TLR3):c.2079A>C (p.Thr693=) rs1362142505
NM_003265.2(TLR3):c.34G>C (p.Gly12Arg) rs199539539
NM_003265.2(TLR3):c.957C>A (p.His319Gln) rs144596374
NM_030930.4(UNC93B1):c.1071C>T (p.Ala357=) rs796106217
NM_030930.4(UNC93B1):c.1090-6C>A rs1168664658
NM_030930.4(UNC93B1):c.135G>A (p.Glu45=) rs572359733
NM_030930.4(UNC93B1):c.1453G>A (p.Val485Met) rs199824078
NM_030930.4(UNC93B1):c.1560G>C (p.Arg520=) rs555389039
NM_030930.4(UNC93B1):c.1629G>A (p.Glu543=) rs576491436
NM_030930.4(UNC93B1):c.1779G>A (p.Gly593=) rs2375183
NM_030930.4(UNC93B1):c.183C>T (p.Leu61=) rs1365228419
NM_030930.4(UNC93B1):c.385C>A (p.Leu129Ile) rs146593182
NM_030930.4(UNC93B1):c.626C>T (p.Pro209Leu) rs144399212
NM_030930.4(UNC93B1):c.642G>A (p.Ala214=) rs201137048
NM_030930.4(UNC93B1):c.87C>T (p.Pro29=) rs937751489
NM_145725.2(TRAF3):c.1254C>T (p.Leu418=) rs201486992
NM_145725.2(TRAF3):c.1323C>T (p.Tyr441=) rs1159024547
NM_145725.2(TRAF3):c.165G>A (p.Lys55=) rs1555373885
NM_145725.2(TRAF3):c.352C>T (p.Arg118Trp) rs143813189
NM_145725.2(TRAF3):c.727-7C>T rs376963322
NM_182919.3(TICAM1):c.1260C>T (p.Gly420=) rs144531955
NM_182919.3(TICAM1):c.1702G>A (p.Ala568Thr) rs143679494
NM_182919.3(TICAM1):c.1755G>A (p.Glu585=) rs1332617784
NM_182919.3(TICAM1):c.330C>T (p.Pro110=) rs373242041
NM_182919.3(TICAM1):c.479C>T (p.Ser160Phe) rs145148929
NM_182919.3(TICAM1):c.549C>T (p.Asp183=) rs759330259
NM_182919.3(TICAM1):c.696C>T (p.Asp232=) rs574449966
NM_182919.3(TICAM1):c.733G>A (p.Gly245Ser) rs151272128
NM_182919.3(TICAM1):c.927A>G (p.Ala309=) rs1555730261

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