List of variants in gene TMPO reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001032283.3(TMPO):c.*1A>G	rs1058300	0.00324
NM_001032283.3(TMPO):c.565+1240G>A	rs139700737	0.00284
NM_001032283.3(TMPO):c.565+1728G>C	rs145703021	0.00188
NM_001032283.3(TMPO):c.565+2224A>G	rs34983516	0.00098
NM_001032283.3(TMPO):c.1119G>A (p.Arg373=)	rs144913822	0.00083
NM_001032283.3(TMPO):c.534T>C (p.Asn178=)	rs200016687	0.00016
NM_001032283.3(TMPO):c.565+2376C>T	rs202035749	0.00015
NM_001032283.3(TMPO):c.565+1301A>G	rs375249647	0.00003
NM_001032283.3(TMPO):c.565+1907A>G	rs372248802	0.00001
NM_001032283.3(TMPO):c.396T>A (p.Gly132=)	rs397516844
NM_001032283.3(TMPO):c.565+2042A>C	rs397516842
NM_001032283.3(TMPO):c.663+13T>G	rs727504798
NM_001032283.3(TMPO):c.681A>G (p.Gly227=)	rs727504733

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