ClinVar Miner

List of variants in gene TDP1 reported by Athena Diagnostics Inc

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Gene type:
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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_018319.4(TDP1):c.1077A>G (p.Pro359=) rs17126522 0.05945
NM_018319.4(TDP1):c.1107T>C (p.Asn369=) rs10151377 0.03424
NM_018319.4(TDP1):c.911G>A (p.Arg304Gln) rs34452707 0.00640
NM_018319.4(TDP1):c.1098A>G (p.Gln366=) rs34563565 0.00639
NM_018319.4(TDP1):c.1705A>G (p.Thr569Ala) rs35973343 0.00413
NM_018319.4(TDP1):c.1536C>T (p.Val512=) rs147837596 0.00227
NM_018319.4(TDP1):c.1165G>A (p.Ala389Thr) rs138044459 0.00178
NM_018319.4(TDP1):c.1800G>A (p.Thr600=) rs75808917 0.00060
NM_018319.4(TDP1):c.1747A>G (p.Ser583Gly) rs201355368 0.00039
NM_018319.4(TDP1):c.1366+10G>A rs200295380 0.00036
NM_018319.4(TDP1):c.774G>A (p.Ala258=) rs139270583 0.00036
NM_018319.4(TDP1):c.1343G>A (p.Arg448Gln) rs144746398 0.00033
NM_018319.4(TDP1):c.1122A>G (p.Arg374=) rs148214612 0.00020
NM_018319.4(TDP1):c.1342C>T (p.Arg448Trp) rs141725364 0.00011
NM_018319.4(TDP1):c.904T>C (p.Tyr302His) rs375817400 0.00010
NM_018319.4(TDP1):c.1249A>G (p.Lys417Glu) rs138135786 0.00009
NM_018319.4(TDP1):c.1543G>A (p.Ala515Thr) rs200769126 0.00009
NM_018319.4(TDP1):c.1312T>A (p.Tyr438Asn) rs182086916 0.00007
NM_018319.4(TDP1):c.1701G>C (p.Met567Ile) rs375084022 0.00005
NM_018319.4(TDP1):c.585G>A (p.Thr195=) rs771269304 0.00004
NM_018319.4(TDP1):c.757G>A (p.Ala253Thr) rs202165305 0.00004
NM_018319.4(TDP1):c.1799C>T (p.Thr600Met) rs772139596 0.00003
NM_018319.4(TDP1):c.716A>G (p.His239Arg) rs750038981 0.00003
NM_018319.4(TDP1):c.1294A>C (p.Lys432Gln) rs202147730 0.00002
NM_018319.4(TDP1):c.1081C>T (p.Arg361Cys) rs368969696 0.00001
NM_018319.4(TDP1):c.1434-9T>C rs768026182 0.00001
NM_018319.4(TDP1):c.802C>G (p.Leu268Val) rs764936943 0.00001
NM_018319.4(TDP1):c.914T>C (p.Ile305Thr) rs367992333 0.00001
NM_018319.4(TDP1):c.1317G>T (p.Leu439Phe) rs138711165
NM_018319.4(TDP1):c.1383C>T (p.Pro461=) rs1433982054
NM_018319.4(TDP1):c.1557G>C (p.Lys519Asn) rs1566913776
NM_018319.4(TDP1):c.1611C>G (p.Tyr537Ter) rs772318046
NM_018319.4(TDP1):c.1731_1753+646del rs1566929134
NM_018319.4(TDP1):c.1735G>A (p.Glu579Lys)
NM_018319.4(TDP1):c.1754-9T>C
NM_018319.4(TDP1):c.1819C>G (p.Pro607Ala)
NM_018319.4(TDP1):c.572C>T (p.Pro191Leu) rs1555383437
NM_018319.4(TDP1):c.621C>T (p.Asp207=) rs746662161
NM_018319.4(TDP1):c.655T>C (p.Phe219Leu)
NM_018319.4(TDP1):c.657C>A (p.Phe219Leu)
NM_018319.4(TDP1):c.876A>T (p.Lys292Asn) rs190449861
NM_018319.4(TDP1):c.970A>T (p.Ile324Phe) rs1555387533
NM_018319.4(TDP1):c.979T>G (p.Leu327Val) rs1555387536
NM_018319.4(TDP1):c.982A>G (p.Met328Val) rs1895351840

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