ClinVar Miner

List of variants in gene TPM1 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 83
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HGVS dbSNP
NC_000015.10:g.63042558A>C
NC_000015.10:g.63042566G>A
NM_001018004.2(TPM1):c.*119T>C rs138843544
NM_001018004.2(TPM1):c.775A>G (p.Lys259Glu) rs144045691
NM_001018005.1(TPM1):c.-206G>A rs17525848
NM_001018005.2(TPM1):c.*148G>T rs7668
NM_001018005.2(TPM1):c.-41C>T rs1335948932
NM_001018005.2(TPM1):c.114+14C>T rs576659891
NM_001018005.2(TPM1):c.115-189G>C rs1057520978
NM_001018005.2(TPM1):c.115-238G>C rs730881126
NM_001018005.2(TPM1):c.115-244G>A rs989115520
NM_001018005.2(TPM1):c.115-298G>A rs786205439
NM_001018005.2(TPM1):c.115-316G>A rs397516491
NM_001018005.2(TPM1):c.115-334C>T rs1392145197
NM_001018005.2(TPM1):c.123T>C (p.Asp41=) rs1029129685
NM_001018005.2(TPM1):c.144G>A (p.Lys48=) rs1555403374
NM_001018005.2(TPM1):c.153G>A (p.Lys51=) rs1555403378
NM_001018005.2(TPM1):c.177A>G (p.Lys59=) rs149346709
NM_001018005.2(TPM1):c.180C>T (p.Tyr60=) rs17850194
NM_001018005.2(TPM1):c.240+11G>A rs367999295
NM_001018005.2(TPM1):c.241-10C>T rs917063084
NM_001018005.2(TPM1):c.241-167A>T
NM_001018005.2(TPM1):c.241-8C>T rs765893032
NM_001018005.2(TPM1):c.241-9T>C rs377417143
NM_001018005.2(TPM1):c.252C>T (p.Asp84=) rs369617788
NM_001018005.2(TPM1):c.27G>A (p.Gln9=) rs397516365
NM_001018005.2(TPM1):c.31C>T (p.Leu11=) rs766883758
NM_001018005.2(TPM1):c.321A>C (p.Ala107=) rs397516368
NM_001018005.2(TPM1):c.374+138A>C
NM_001018005.2(TPM1):c.375-17C>T rs1057523797
NM_001018005.2(TPM1):c.375-262G>A
NM_001018005.2(TPM1):c.375-311C>T
NM_001018005.2(TPM1):c.375-3C>T rs202228866
NM_001018005.2(TPM1):c.375-5T>C rs377061868
NM_001018005.2(TPM1):c.444G>C (p.Leu148=) rs376518788
NM_001018005.2(TPM1):c.453C>A (p.Ala151=) rs1071646
NM_001018005.2(TPM1):c.486T>C (p.Tyr162=) rs11558747
NM_001018005.2(TPM1):c.493-110T>C
NM_001018005.2(TPM1):c.522C>T (p.Ser174=) rs200173919
NM_001018005.2(TPM1):c.546G>A (p.Arg182=) rs1555409143
NM_001018005.2(TPM1):c.549T>C (p.Ala183=) rs199476313
NM_001018005.2(TPM1):c.555C>T (p.Leu185=) rs752088217
NM_001018005.2(TPM1):c.563+10C>T rs397516377
NM_001018005.2(TPM1):c.563+12C>T rs756230680
NM_001018005.2(TPM1):c.563+243C>T
NM_001018005.2(TPM1):c.563+284T>C rs1566964956
NM_001018005.2(TPM1):c.563+332A>G rs1566965048
NM_001018005.2(TPM1):c.563+347C>T rs759081217
NM_001018005.2(TPM1):c.563+348G>T rs397516381
NM_001018005.2(TPM1):c.563+6C>A rs397516378
NM_001018005.2(TPM1):c.563+7G>A rs374563216
NM_001018005.2(TPM1):c.564-11G>A rs532254032
NM_001018005.2(TPM1):c.564-12C>T rs113591254
NM_001018005.2(TPM1):c.564-47C>T
NM_001018005.2(TPM1):c.573C>T (p.Ala191=) rs780507307
NM_001018005.2(TPM1):c.603G>C (p.Thr201=) rs397516485
NM_001018005.2(TPM1):c.606C>T (p.Asn202=) rs1225777387
NM_001018005.2(TPM1):c.630G>A (p.Gln210=) rs761816813
NM_001018005.2(TPM1):c.639+10G>A rs763272536
NM_001018005.2(TPM1):c.639+13del rs397516488
NM_001018005.2(TPM1):c.639+22G>C
NM_001018005.2(TPM1):c.684T>C (p.Leu228=) rs397516384
NM_001018005.2(TPM1):c.687C>T (p.Ser229=) rs759362606
NM_001018005.2(TPM1):c.702+10G>C rs1386461337
NM_001018005.2(TPM1):c.702+7del rs1060504368
NM_001018005.2(TPM1):c.705T>C (p.Ala235=) rs1222579354
NM_001018005.2(TPM1):c.726G>A (p.Ala242=) rs200484871
NM_001018005.2(TPM1):c.768A>G (p.Leu256=) rs139650306
NM_001018005.2(TPM1):c.773-18T>C rs759150466
NM_001018005.2(TPM1):c.773-233G>A
NM_001018005.2(TPM1):c.773-4A>G rs1555410410
NM_001018005.2(TPM1):c.775G>C (p.Glu259Gln) rs397516389
NM_001018005.2(TPM1):c.783C>T (p.Tyr261=) rs751001221
NM_001018005.2(TPM1):c.828C>T (p.His276=) rs368813394
NM_001018005.2(TPM1):c.837C>T (p.Asn279=) rs397516393
NM_001018005.2(TPM1):c.845C>G (p.Thr282Ser) rs397516395
NM_001018005.2(TPM1):c.851+189C>G
NM_001018005.2(TPM1):c.851+233G>A
NM_001018005.2(TPM1):c.851+6C>A rs375043184
NM_001018005.2(TPM1):c.851+6C>T rs375043184
NM_001018008.2(TPM1):c.*1209C>T rs374434837
NM_001018008.2(TPM1):c.*1223C>T rs1057521824
NM_001018008.2(TPM1):c.695G>A (p.Arg232His) rs730881128

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