ClinVar Miner

List of variants in gene TPM1 reported as likely benign for Cardiovascular phenotype

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001018005.2(TPM1):c.180C>T (p.Tyr60=) rs17850194 0.00273
NM_001018005.2(TPM1):c.177A>G (p.Lys59=) rs149346709 0.00031
NM_001018005.2(TPM1):c.797A>G (p.Lys266Arg) rs371934474 0.00021
NM_001018005.2(TPM1):c.726G>A (p.Ala242=) rs200484871 0.00011
NM_001018005.2(TPM1):c.522C>T (p.Ser174=) rs200173919 0.00010
NM_001018005.2(TPM1):c.27G>A (p.Gln9=) rs397516365 0.00006
NM_001018005.2(TPM1):c.687C>T (p.Ser229=) rs759362606 0.00004
NM_001018005.2(TPM1):c.783C>T (p.Tyr261=) rs751001221 0.00004
NM_001018005.2(TPM1):c.474C>T (p.Ala158=) rs143922069 0.00003
NM_001018005.2(TPM1):c.549T>C (p.Ala183=) rs199476313 0.00003
NM_001018005.2(TPM1):c.845C>G (p.Thr282Ser) rs397516395 0.00003
NM_001018005.2(TPM1):c.645G>A (p.Ser215=) rs773403386 0.00002
NM_001018005.2(TPM1):c.663T>C (p.Tyr221=) rs774859181 0.00002
NM_001018005.2(TPM1):c.252C>T (p.Asp84=) rs369617788 0.00001
NM_001018005.2(TPM1):c.273C>T (p.Arg91=) rs1400074860 0.00001
NM_001018005.2(TPM1):c.288G>A (p.Glu96=) rs192883939 0.00001
NM_001018005.2(TPM1):c.438C>T (p.Ile146=) rs1460142862 0.00001
NM_001018005.2(TPM1):c.555C>T (p.Leu185=) rs752088217 0.00001
NM_001018005.2(TPM1):c.573C>T (p.Ala191=) rs780507307 0.00001
NM_001018005.2(TPM1):c.684T>C (p.Leu228=) rs397516384 0.00001
NM_001018005.2(TPM1):c.705T>C (p.Ala235=) rs1222579354 0.00001
NM_001018005.2(TPM1):c.807C>T (p.Ala269=) rs751778912 0.00001
NM_001018005.2(TPM1):c.828C>T (p.His276=) rs368813394 0.00001
NM_001018005.2(TPM1):c.837C>T (p.Asn279=) rs397516393 0.00001
NM_001018005.2(TPM1):c.93G>C (p.Ala31=) rs770661916 0.00001
NM_001018005.2(TPM1):c.207G>A (p.Glu69=)
NM_001018005.2(TPM1):c.213G>A (p.Leu71=)
NM_001018005.2(TPM1):c.328T>C (p.Leu110=)
NM_001018005.2(TPM1):c.336G>A (p.Lys112=)
NM_001018005.2(TPM1):c.33G>C (p.Leu11=)
NM_001018005.2(TPM1):c.48G>A (p.Glu16=)
NM_001018005.2(TPM1):c.589T>C (p.Leu197=) rs2140963629
NM_001018005.2(TPM1):c.681C>T (p.Val227=)
NM_001018005.2(TPM1):c.717T>G (p.Ala239=)
NM_001018005.2(TPM1):c.813C>T (p.Ser271=)
NM_001018005.2(TPM1):c.87G>A (p.Lys29=) rs530234301
NM_001018005.2(TPM1):c.93G>A (p.Ala31=)

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.