ClinVar Miner

List of variants in gene TPM1 reported as likely benign for Hypertrophic cardiomyopathy

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Gene type:
ClinVar version:
Total variants: 18
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NM_001018004.2(TPM1):c.*119T>C rs138843544
NM_001018005.1(TPM1):c.-206G>A rs17525848
NM_001018005.2(TPM1):c.*148G>T rs7668
NM_001018005.2(TPM1):c.123T>C (p.Asp41=) rs1029129685
NM_001018005.2(TPM1):c.153G>A (p.Lys51=) rs1555403378
NM_001018005.2(TPM1):c.241-10C>T rs917063084
NM_001018005.2(TPM1):c.241-8C>T rs765893032
NM_001018005.2(TPM1):c.252C>T (p.Asp84=) rs369617788
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.546G>A (p.Arg182=) rs1555409143
NM_001018005.2(TPM1):c.549T>C (p.Ala183=) rs199476313
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.687C>T (p.Ser229=) rs759362606
NM_001018005.2(TPM1):c.702+10G>C rs1386461337
NM_001018005.2(TPM1):c.773-4A>G rs1555410410

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