List of variants in gene TDP1 reported as uncertain significance for cerebellar ataxia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 51

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HGVS	dbSNP	gnomAD frequency
NM_018319.3(TDP1):c.-292G>T	rs577403021	0.00332
NM_018319.4(TDP1):c.*496G>A	rs34796911	0.00305
NM_018319.4(TDP1):c.*945C>T	rs540904390	0.00051
NM_018319.4(TDP1):c.1747A>G (p.Ser583Gly)	rs201355368	0.00039
NM_018319.4(TDP1):c.*950C>T	rs577840358	0.00035
NM_018319.4(TDP1):c.1343G>A (p.Arg448Gln)	rs144746398	0.00033
NM_018319.4(TDP1):c.*1355G>A	rs755484553	0.00022
NM_018319.4(TDP1):c.884+5G>A	rs370991229	0.00022
NM_018319.4(TDP1):c.*1203G>T	rs531417402	0.00018
NM_018319.4(TDP1):c.*228T>G	rs954549405	0.00018
NM_018319.4(TDP1):c.885-15T>C	rs375601290	0.00016
NM_018319.4(TDP1):c.*1015G>A	rs374734859	0.00011
NM_018319.4(TDP1):c.1342C>T (p.Arg448Trp)	rs141725364	0.00011
NM_018319.4(TDP1):c.*801G>A	rs1017363264	0.00010
NM_018319.4(TDP1):c.*776T>C	rs761481355	0.00009
NM_018319.4(TDP1):c.-8+15T>C	rs767166629	0.00008
NM_018319.4(TDP1):c.*904C>T	rs886050884	0.00006
NM_018319.4(TDP1):c.789C>T (p.His263=)	rs562317662	0.00006
NM_018319.4(TDP1):c.*1200G>A	rs758892109	0.00004
NM_018319.4(TDP1):c.*37T>C	rs374710359	0.00004
NM_018319.4(TDP1):c.757G>A (p.Ala253Thr)	rs202165305	0.00004
NM_018319.4(TDP1):c.*264G>T	rs779122283	0.00003
NM_018319.4(TDP1):c.*631C>T	rs1027214918	0.00003
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.998C>T (p.Pro333Leu)	rs142600338	0.00003
NM_018319.4(TDP1):c.-232A>C	rs886050882	0.00002
NM_018319.4(TDP1):c.1527G>C (p.Trp509Cys)	rs369742694	0.00002
NM_018319.4(TDP1):c.1793C>T (p.Pro598Leu)	rs113382706	0.00002
NM_018319.3(TDP1):c.-278C>T	rs886050880	0.00001
NM_018319.4(TDP1):c.*1239T>C	rs1387359215	0.00001
NM_018319.4(TDP1):c.*1367A>G	rs1462755052	0.00001
NM_018319.4(TDP1):c.*774G>A	rs372910082	0.00001
NM_018319.4(TDP1):c.-38G>A	rs1037056557	0.00001
NM_018319.4(TDP1):c.643T>C (p.Tyr215His)	rs754702237	0.00001
NM_018319.4(TDP1):c.896del (p.Ser299fs)	rs773960264	0.00001
NM_018319.3(TDP1):c.-275C>G	rs886050881
NM_018319.4(TDP1):c.*1099G>A	rs1888617977
NM_018319.4(TDP1):c.*134A>C	rs780471860
NM_018319.4(TDP1):c.*135T>C	rs1566938109
NM_018319.4(TDP1):c.*1399T>A	rs1888638490
NM_018319.4(TDP1):c.*1511C>G	rs1596750474
NM_018319.4(TDP1):c.-242T>G	rs533696578
NM_018319.4(TDP1):c.-243C>T	rs886873955
NM_018319.4(TDP1):c.-264G>A	rs1891509764
NM_018319.4(TDP1):c.-55C>G	rs751280891
NM_018319.4(TDP1):c.-76T>C	rs886050883
NM_018319.4(TDP1):c.1201G>T (p.Val401Phe)	rs892739281
NM_018319.4(TDP1):c.1317G>T (p.Leu439Phe)	rs138711165
NM_018319.4(TDP1):c.1611C>G (p.Tyr537Ter)	rs772318046
NM_018319.4(TDP1):c.764T>G (p.Leu255Trp)	rs151271332

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