List of variants in gene TMPO reported as uncertain significance by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001032283.3(TMPO):c.358C>A (p.Leu120Ile)	rs200420073	0.00029
NM_001032283.3(TMPO):c.565+1531C>T	rs199943517	0.00009
NM_001032283.3(TMPO):c.887A>G (p.Asn296Ser)	rs771589075	0.00006
NM_001032283.3(TMPO):c.565+1824C>G	rs373861992	0.00005
NM_001032283.3(TMPO):c.565+1675A>G	rs370366685	0.00004
NM_001032283.3(TMPO):c.856A>G (p.Met286Val)	rs199594991	0.00004
NM_001032283.3(TMPO):c.1177A>G (p.Lys393Glu)	rs199545670	0.00003
NM_001032283.3(TMPO):c.1120C>A (p.Pro374Thr)	rs778140094	0.00001
NM_001032283.3(TMPO):c.382G>A (p.Gly128Arg)	rs200943582	0.00001
NM_001032283.3(TMPO):c.557A>G (p.Asn186Ser)	rs200923649	0.00001
NM_001032283.3(TMPO):c.565+1305T>G	rs201730568	0.00001
NM_001032283.3(TMPO):c.331G>A (p.Asp111Asn)	rs201838047
NM_001032283.3(TMPO):c.565+2439A>G	rs200419485

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.