List of variants in gene TDP1 reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_018319.4(TDP1):c.1747A>G (p.Ser583Gly)	rs201355368	0.00039
NM_018319.4(TDP1):c.1343G>A (p.Arg448Gln)	rs144746398	0.00033
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.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.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.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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