ClinVar Miner

List of variants in gene TDP1 reported as benign for cerebellar disorder

Included ClinVar conditions (275):
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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_018319.4(TDP1):c.-230-14C>A rs28365055 0.25524
NM_018319.4(TDP1):c.*77C>T rs9488 0.20063
NM_018319.4(TDP1):c.-21C>T rs34348197 0.06559
NM_018319.4(TDP1):c.*1448G>A rs34004710 0.05962
NM_018319.4(TDP1):c.*1452C>T rs34923595 0.05957
NM_018319.4(TDP1):c.*1460C>G rs35944390 0.05950
NM_018319.4(TDP1):c.1077A>G (p.Pro359=) rs17126522 0.05945
NM_018319.4(TDP1):c.-224A>G rs35439694 0.05316
NM_018319.4(TDP1):c.-177C>T rs35132667 0.04596
NM_018319.4(TDP1):c.1107T>C (p.Asn369=) rs10151377 0.03424
NM_018319.4(TDP1):c.*393T>C rs7150480 0.03142
NM_018319.4(TDP1):c.*539G>A rs35090050 0.02032
NM_018319.4(TDP1):c.-230-4G>T rs28365053 0.01666
NM_018319.4(TDP1):c.*799A>G rs35437984 0.01042
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.*1105A>G rs34815305 0.00542
NM_018319.4(TDP1):c.*598G>A rs34083314 0.00430
NM_018319.4(TDP1):c.1317+11G>A rs36009827 0.00423
NM_018319.4(TDP1):c.1705A>G (p.Thr569Ala) rs35973343 0.00413
NM_018319.4(TDP1):c.1165G>A (p.Ala389Thr) rs138044459 0.00178
NM_018319.3(TDP1):c.-276_-274dupCCG rs35210768
NM_018319.4(TDP1):c.*608del rs397897279

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