ClinVar Miner

List of variants in gene TDP1 reported as uncertain significance for DNA repair disease

Included ClinVar conditions (106):
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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP
NM_018319.3(TDP1):c.-275C>G rs886050881
NM_018319.3(TDP1):c.-278C>T rs886050880
NM_018319.3(TDP1):c.-292G>T rs577403021
NM_018319.4(TDP1):c.*1015G>A rs374734859
NM_018319.4(TDP1):c.*1099G>A
NM_018319.4(TDP1):c.*1200G>A
NM_018319.4(TDP1):c.*1203G>T rs531417402
NM_018319.4(TDP1):c.*1239T>C
NM_018319.4(TDP1):c.*134A>C
NM_018319.4(TDP1):c.*1355G>A rs755484553
NM_018319.4(TDP1):c.*135T>C
NM_018319.4(TDP1):c.*1367A>G
NM_018319.4(TDP1):c.*1399T>A
NM_018319.4(TDP1):c.*1511C>G
NM_018319.4(TDP1):c.*228T>G
NM_018319.4(TDP1):c.*264G>T rs779122283
NM_018319.4(TDP1):c.*37T>C
NM_018319.4(TDP1):c.*496G>A
NM_018319.4(TDP1):c.*631C>T
NM_018319.4(TDP1):c.*774G>A rs372910082
NM_018319.4(TDP1):c.*776T>C rs761481355
NM_018319.4(TDP1):c.*801G>A
NM_018319.4(TDP1):c.*904C>T rs886050884
NM_018319.4(TDP1):c.*945C>T rs540904390
NM_018319.4(TDP1):c.*950C>T
NM_018319.4(TDP1):c.-242T>G
NM_018319.4(TDP1):c.-243C>T
NM_018319.4(TDP1):c.-264G>A
NM_018319.4(TDP1):c.-38G>A
NM_018319.4(TDP1):c.-55C>G rs751280891
NM_018319.4(TDP1):c.-76T>C rs886050883
NM_018319.4(TDP1):c.-8+15T>C
NM_018319.4(TDP1):c.1201G>T (p.Val401Phe)
NM_018319.4(TDP1):c.1342C>T (p.Arg448Trp) rs141725364
NM_018319.4(TDP1):c.1343G>A (p.Arg448Gln) rs144746398
NM_018319.4(TDP1):c.137A>G (p.Tyr46Cys) rs141387488
NM_018319.4(TDP1):c.1527G>C (p.Trp509Cys)
NM_018319.4(TDP1):c.15C>T (p.Gly5=) rs779666160
NM_018319.4(TDP1):c.1611C>G (p.Tyr537Ter) rs772318046
NM_018319.4(TDP1):c.1747A>G (p.Ser583Gly) rs201355368
NM_018319.4(TDP1):c.1799C>T (p.Thr600Met) rs772139596
NM_018319.4(TDP1):c.19T>C (p.Tyr7His) rs754747710
NM_018319.4(TDP1):c.208T>A (p.Ser70Thr) rs140058160
NM_018319.4(TDP1):c.236G>C (p.Ser79Thr) rs148927677
NM_018319.4(TDP1):c.25A>G (p.Arg9Gly)
NM_018319.4(TDP1):c.353C>T (p.Ala118Val)
NM_018319.4(TDP1):c.643T>C (p.Tyr215His)
NM_018319.4(TDP1):c.68C>T (p.Pro23Leu)
NM_018319.4(TDP1):c.716A>G (p.His239Arg) rs750038981
NM_018319.4(TDP1):c.757G>A (p.Ala253Thr)
NM_018319.4(TDP1):c.789C>T (p.His263=) rs562317662
NM_018319.4(TDP1):c.84A>G (p.Pro28=)
NM_018319.4(TDP1):c.884+5G>A rs370991229
NM_018319.4(TDP1):c.885-15T>C rs375601290
NM_018319.4(TDP1):c.896del (p.Ser299fs) rs773960264
NM_018319.4(TDP1):c.998C>T (p.Pro333Leu)

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