ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_001018005.2(TPM1):c.180C>T (p.Tyr60=) rs17850194 0.00273
NM_001018004.2(TPM1):c.775A>G (p.Lys259Glu) rs144045691 0.00052
NM_001018005.2(TPM1):c.375-5T>C rs377061868 0.00029
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.522C>T (p.Ser174=) rs200173919 0.00010
NM_001018005.2(TPM1):c.563+12C>T rs756230680 0.00009
NM_001018005.2(TPM1):c.27G>A (p.Gln9=) rs397516365 0.00006
NM_001018005.2(TPM1):c.493-18T>G rs377726678 0.00006
NM_001018005.2(TPM1):c.563+7G>A rs374563216 0.00006
NM_001018008.2(TPM1):c.695G>A (p.Arg232His) rs730881128 0.00006
NM_001018005.2(TPM1):c.783C>T (p.Tyr261=) rs751001221 0.00004
NM_001018005.2(TPM1):c.375-3C>T rs202228866 0.00003
NM_001018005.2(TPM1):c.549T>C (p.Ala183=) rs199476313 0.00003
NM_001018005.2(TPM1):c.563+347C>T rs759081217 0.00003
NM_001018005.2(TPM1):c.564-12C>T rs113591254 0.00003
NM_001018005.2(TPM1):c.240+11G>A rs367999295 0.00002
NM_001018005.2(TPM1):c.31C>T (p.Leu11=) rs766883758 0.00002
NM_001018005.2(TPM1):c.-41C>T rs1335948932 0.00001
NM_001018005.2(TPM1):c.241-9T>C rs377417143 0.00001
NM_001018005.2(TPM1):c.252C>T (p.Asp84=) rs369617788 0.00001
NM_001018005.2(TPM1):c.444G>C (p.Leu148=) rs376518788 0.00001
NM_001018005.2(TPM1):c.639+10G>A rs763272536 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.768A>G (p.Leu256=) rs139650306 0.00001
NM_001018005.2(TPM1):c.773-18T>C rs759150466 0.00001
NM_001018005.2(TPM1):c.837C>T (p.Asn279=) rs397516393 0.00001
NM_000366.2(TPM1):c.849C>T (p.Asn283=) rs1057521824
NM_001018005.2(TPM1):c.115-298G>A rs786205439
NM_001018005.2(TPM1):c.144G>A (p.Lys48=) rs1555403374
NM_001018005.2(TPM1):c.294G>A (p.Glu98=) rs747206706
NM_001018005.2(TPM1):c.321A>C (p.Ala107=) rs397516368
NM_001018005.2(TPM1):c.375-17C>T rs1057523797
NM_001018005.2(TPM1):c.563+10C>T rs397516377
NM_001018005.2(TPM1):c.563+348G>T rs397516381
NM_001018005.2(TPM1):c.563+353G>T
NM_001018005.2(TPM1):c.563+6C>A rs397516378
NM_001018005.2(TPM1):c.603G>C (p.Thr201=) rs397516485
NM_001018005.2(TPM1):c.639+13del rs397516488
NM_001018005.2(TPM1):c.775G>C (p.Glu259Gln) rs397516389

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