List of variants in gene TMPO reported as benign for not provided

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: 36

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001032283.3(TMPO):c.565+34G>T	rs3213901	0.57425
NM_001032283.3(TMPO):c.407-203T>C	rs61934004	0.57054
NM_001032283.3(TMPO):c.280-321C>T	rs7135956	0.35398
NM_001032283.3(TMPO):c.280-131G>T	rs7136406	0.35369
NM_001032283.3(TMPO):c.566-289C>T	rs11109522	0.21983
NM_001032283.3(TMPO):c.990+333G>A	rs11109524	0.21982
NM_001032283.3(TMPO):c.280-90G>T	rs11109517	0.21979
NM_001032283.3(TMPO):c.1080-128A>G	rs10860342	0.21973
NM_001032283.3(TMPO):c.280-102A>G	rs35124796	0.19353
NM_001032283.3(TMPO):c.565+249C>A	rs3213900	0.19097
NM_001032283.3(TMPO):c.565+748T>C	rs73384409	0.12146
NM_001032283.3(TMPO):c.990+281T>C	rs2068060	0.09530
NM_001032283.3(TMPO):c.663+178T>C	rs12825374	0.07002
NM_001032283.3(TMPO):c.990+72_990+73insG	rs201498123	0.05605
NM_001032283.3(TMPO):c.566-142T>C	rs34646198	0.04042
NM_001032283.3(TMPO):c.280-286A>T	rs12311323	0.03437
NM_001032283.3(TMPO):c.407-96G>C	rs17028432	0.02747
NM_001032283.3(TMPO):c.565+1665A>G	rs11838270	0.02179
NM_001032283.3(TMPO):c.991-4T>C	rs112475937	0.01905
NM_001032283.3(TMPO):c.859G>C (p.Ala287Pro)	rs7133258	0.00977
NM_001032283.3(TMPO):c.565+2487C>T	rs17028450	0.00576
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+1105C>T	rs138790561	0.00038
NM_001032283.3(TMPO):c.13C>T (p.Leu5=)	rs149067616	0.00005
NM_001032283.3(TMPO):c.1079+5dup	rs34449077
NM_001032283.3(TMPO):c.284C>A (p.Ala95Asp)	rs1565808154
NM_001032283.3(TMPO):c.565+816_565+817del	rs201794513
NM_001032283.3(TMPO):c.879+112_879+113dup	rs34340378
NM_001032283.3(TMPO):c.879+113del	rs34340378
NM_001032283.3(TMPO):c.879+113dup	rs34340378
NM_001032283.3(TMPO):c.990+84_990+86dup	rs79128220
NM_001032283.3(TMPO):c.990+86del	rs79128220
NM_001032283.3(TMPO):c.990+86dup	rs79128220
NM_001032283.3(TMPO):c.991-299C>A	rs11109525
NM_003276.2(TMPO):c.-439C>T	rs117151045

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.