ClinVar Miner

List of variants in gene TLR3 reported as uncertain significance for Herpesviridae infectious disease

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NC_000004.11:g.(?_186997754)_(187006047_?)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

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