List of variants in gene TPM1 reported by Stanford Center for Inherited Cardiovascular Disease, Stanford University

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001018008.2(TPM1):c.695G>A (p.Arg232His)	rs730881128	0.00006
NM_001018005.2(TPM1):c.845C>G (p.Thr282Ser)	rs397516395	0.00003
NM_001018005.2(TPM1):c.644C>T (p.Ser215Leu)	rs199476316	0.00001
NM_001018005.2(TPM1):c.64G>A (p.Ala22Thr)	rs397516382	0.00001
NM_001018005.2(TPM1):c.850A>G (p.Ile284Val)	rs199476322	0.00001
NM_001018005.2(TPM1):c.115-238G>C	rs730881126
NM_001018005.2(TPM1):c.253G>T (p.Val85Leu)	rs730881156
NM_001018005.2(TPM1):c.389T>C (p.Ile130Thr)	rs727503517
NM_001018005.2(TPM1):c.574G>A (p.Glu192Lys)	rs199476315
NM_001018005.2(TPM1):c.637A>C (p.Lys213Gln)	rs1566966003
NM_001018005.2(TPM1):c.688G>A (p.Asp230Asn)	rs199476317
NM_001018005.2(TPM1):c.69G>C (p.Glu23Asp)	rs876661396
NM_001018005.2(TPM1):c.712C>T (p.Arg238Trp)	rs397516386
NM_001018005.2(TPM1):c.715G>A (p.Ala239Thr)	rs199476318
NM_001018005.2(TPM1):c.762T>A (p.Asp254Glu)	rs727504354
NM_001018005.2(TPM1):c.835A>C (p.Asn279His)	rs397516392

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