ClinVar Miner

List of variants in gene TPM1 reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
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.177A>G (p.Lys59=) rs149346709
NM_001018005.2(TPM1):c.241-10C>T rs917063084
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.375-5T>C rs377061868
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.563+7G>A rs374563216
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.702+7del rs1060504368
NM_001018005.2(TPM1):c.726G>A (p.Ala242=) rs200484871
NM_001018005.2(TPM1):c.773-4A>G rs1555410410
NM_001018005.2(TPM1):c.845C>G (p.Thr282Ser) rs397516395

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