ClinVar Miner

List of variants in gene TPM1 reported as likely benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_000366.5(TPM1):c.375-3C>T rs202228866
NM_000366.5(TPM1):c.768A>G (p.Leu256=) rs139650306
NM_001018004.1(TPM1):c.775A>G (p.Lys259Glu) rs144045691
NM_001018005.1(TPM1):c.*4001G>A rs730881128
NM_001018005.1(TPM1):c.114+14C>T rs576659891
NM_001018005.1(TPM1):c.115-316G>A rs397516491
NM_001018005.1(TPM1):c.241-9T>C rs377417143
NM_001018005.1(TPM1):c.252C>T (p.Asp84=) rs369617788
NM_001018005.1(TPM1):c.27G>A (p.Gln9=) rs397516365
NM_001018005.1(TPM1):c.321A>C (p.Ala107=) rs397516368
NM_001018005.1(TPM1):c.375-5T>C rs377061868
NM_001018005.1(TPM1):c.444G>C (p.Leu148=) rs376518788
NM_001018005.1(TPM1):c.522C>T (p.Ser174=) rs200173919
NM_001018005.1(TPM1):c.549T>C (p.Ala183=) rs199476313
NM_001018005.1(TPM1):c.563+10C>T rs397516377
NM_001018005.1(TPM1):c.563+348G>T rs397516381
NM_001018005.1(TPM1):c.563+6C>A rs397516378
NM_001018005.1(TPM1):c.603G>C (p.Thr201=) rs397516485
NM_001018005.1(TPM1):c.639+13delG rs397516488
NM_001018005.1(TPM1):c.684T>C (p.Leu228=) rs397516384
NM_001018005.1(TPM1):c.726G>A (p.Ala242=) rs200484871
NM_001018005.1(TPM1):c.837C>T (p.Asn279=) rs397516393
NM_001018020.1(TPM1):c.138G>A (p.Lys46=) rs786205439

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