List of variants in gene TPM1 reported as benign for not specified

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: 27

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001018005.2(TPM1):c.453C>A (p.Ala151=)	rs1071646	0.64628
NM_001018005.2(TPM1):c.486T>C (p.Tyr162=)	rs11558747	0.05001
NM_001018005.2(TPM1):c.851+99dup	rs201411148	0.00955
NM_001018005.2(TPM1):c.639+22G>C	rs28730802	0.00782
NM_001018020.2(TPM1):c.*31G>A	rs11558748	0.00598
NM_001018005.2(TPM1):c.180C>T (p.Tyr60=)	rs17850194	0.00273
NM_001018005.2(TPM1):c.115-262C>T	rs74573041	0.00079
NM_001018005.2(TPM1):c.115-319C>G	rs201720832	0.00070
NM_001018004.2(TPM1):c.775A>G (p.Lys259Glu)	rs144045691	0.00052
NM_001018005.2(TPM1):c.639+21G>C	rs199989220	0.00041
NM_001018005.2(TPM1):c.375-5T>C	rs377061868	0.00029
NM_001018005.2(TPM1):c.563+313A>G	rs144700226	0.00029
NM_001018005.2(TPM1):c.240+21C>T	rs201979210	0.00021
NM_001018005.2(TPM1):c.115-316G>A	rs397516491	0.00015
NM_001018005.2(TPM1):c.114+14C>T	rs576659891	0.00014
NM_001018005.2(TPM1):c.726G>A (p.Ala242=)	rs200484871	0.00011
NM_001018005.2(TPM1):c.851+33C>T	rs376843038	0.00009
NM_001018005.2(TPM1):c.564-11G>A	rs532254032	0.00007
NM_001018005.2(TPM1):c.115-335G>T	rs587780971	0.00006
NM_001018005.2(TPM1):c.27G>A (p.Gln9=)	rs397516365	0.00006
NM_001018005.2(TPM1):c.241-8C>T	rs765893032	0.00003
NM_001018005.2(TPM1):c.375-3C>T	rs202228866	0.00003
NM_001018005.2(TPM1):c.115-277G>A	rs1312883932
NM_001018005.2(TPM1):c.374+65del	rs146241142
NM_001018005.2(TPM1):c.45G>A (p.Lys15=)	rs199476301
NM_001018005.2(TPM1):c.61C>A (p.Arg21=)	rs1437698471
NM_001018005.2(TPM1):c.639+13del	rs397516488

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.