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

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 18

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HGVS	dbSNP
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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