List of variants in gene TPM1 reported as likely pathogenic for Primary dilated cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001018005.2(TPM1):c.163G>A (p.Asp55Asn)	rs397516363
NM_001018005.2(TPM1):c.23T>G (p.Met8Arg)	rs397516364
NM_001018005.2(TPM1):c.275T>C (p.Ile92Thr)	rs199476310
NM_001018005.2(TPM1):c.337C>G (p.Leu113Val)	rs397516369
NM_001018005.2(TPM1):c.341A>G (p.Glu114Gly)	rs397516370
NM_001018005.2(TPM1):c.416A>T (p.Glu139Val)	rs727504389
NM_001018005.2(TPM1):c.423G>C (p.Met141Ile)	rs397516371
NM_001018005.2(TPM1):c.475G>A (p.Asp159Asn)	rs397516373
NM_001018005.2(TPM1):c.479G>A (p.Arg160His)	rs199476311
NM_001018005.2(TPM1):c.496G>A (p.Ala166Thr)	rs876657662
NM_001018005.2(TPM1):c.725C>T (p.Ala242Val)	rs397516387

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