ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_001018005.1(TPM1):c.*5253C>T rs374434837
NM_001018005.1(TPM1):c.*5267C>T rs1057521824
NM_001018005.1(TPM1):c.-41C>T rs1335948932
NM_001018005.1(TPM1):c.115-189G>C rs1057520978
NM_001018005.1(TPM1):c.115-244G>A rs989115520
NM_001018005.1(TPM1):c.144G>A (p.Lys48=) rs1555403374
NM_001018005.1(TPM1):c.240+11G>A rs367999295
NM_001018005.1(TPM1):c.31C>T (p.Leu11=) rs766883758
NM_001018005.1(TPM1):c.375-17C>T rs1057523797
NM_001018005.1(TPM1):c.563+12C>T rs756230680
NM_001018005.1(TPM1):c.563+347C>T rs759081217
NM_001018005.1(TPM1):c.563+7G>A rs374563216
NM_001018005.1(TPM1):c.564-12C>T rs113591254
NM_001018005.1(TPM1):c.639+10G>A rs763272536
NM_001018005.1(TPM1):c.705T>C (p.Ala235=) rs1222579354
NM_001018005.1(TPM1):c.773-18T>C rs759150466
NM_001018005.1(TPM1):c.775G>C (p.Glu259Gln) rs397516389
NM_001018005.1(TPM1):c.783C>T (p.Tyr261=) rs751001221
NM_001018005.1(TPM1):c.851+6C>A rs375043184
NM_001018005.1(TPM1):c.851+6C>T rs375043184
NM_001018020.1(TPM1):c.198G>C (p.Lys66Asn) rs730881126

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