ClinVar Miner

List of variants reported as benign for Herpesviridae infectious disease

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 32
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HGVS dbSNP
NM_003265.2(TLR3):c.1234C>T (p.Leu412Phe) rs3775291
NM_003265.2(TLR3):c.1677G>A (p.Lys559=) rs35617964
NM_003265.2(TLR3):c.1704C>T (p.Asn568=) rs35111588
NM_003265.2(TLR3):c.1927C>A (p.Arg643Ser) rs73025939
NM_003265.2(TLR3):c.2209T>A (p.Ser737Thr) rs5743318
NM_003265.2(TLR3):c.2553C>T (p.Phe851=) rs73873710
NM_003265.2(TLR3):c.2556T>G (p.Leu852=) rs115677523
NM_003265.2(TLR3):c.634-10C>A rs113654222
NM_003265.2(TLR3):c.727T>C (p.Leu243=) rs75290011
NM_003265.2(TLR3):c.838G>A (p.Asp280Asn) rs112077022
NM_003265.2(TLR3):c.919T>G (p.Tyr307Asp) rs5743317
NM_003300.4(TRAF3):c.245+10_245+21del rs567455701
NM_030930.4(UNC93B1):c.1090-10dup rs760132599
NM_030930.4(UNC93B1):c.1155C>T (p.Gly385=) rs200930438
NM_030930.4(UNC93B1):c.1163C>T (p.Ala388Val) rs11543208
NM_030930.4(UNC93B1):c.1206G>C (p.Pro402=) rs112284414
NM_030930.4(UNC93B1):c.1557C>G (p.Arg519=) rs7149
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.239-6C>T rs182093266
NM_030930.4(UNC93B1):c.393-10C>T rs117183629
NM_030930.4(UNC93B1):c.907-5C>T rs144979304
NM_145725.2(TRAF3):c.1110C>T (p.Ser370=) rs1051743
NM_145725.2(TRAF3):c.1509C>T (p.Ser503=) rs138943371
NM_145725.2(TRAF3):c.189G>A (p.Pro63=) rs142350527
NM_145725.2(TRAF3):c.449G>A (p.Arg150His) rs141920055
NM_145725.2(TRAF3):c.727-5C>T rs767004037
NM_182919.3(TICAM1):c.1763A>C (p.Gln588Pro) rs199784356
NM_182919.3(TICAM1):c.1803G>A (p.Ala601=) rs11466723
NM_182919.3(TICAM1):c.223C>T (p.Arg75Cys) rs11466719
NM_182919.3(TICAM1):c.306G>A (p.Leu102=) rs11466720
NM_182919.3(TICAM1):c.95C>T (p.Thr32Ile) rs79591246

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