List of variants in gene TPM1 reported as pathogenic for cardiovascular disorder

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_001018005.2(TPM1):c.523G>A (p.Asp175Asn)	rs104894503	0.00003
NM_001018005.2(TPM1):c.644C>T (p.Ser215Leu)	rs199476316	0.00001
NM_001018005.2(TPM1):c.842T>C (p.Met281Thr)	rs199476321	0.00001
NM_001018005.2(TPM1):c.118G>A (p.Glu40Lys)	rs104894501
NM_001018005.2(TPM1):c.160G>A (p.Glu54Lys)	rs104894505
NM_001018005.2(TPM1):c.188C>T (p.Ala63Val)	rs199476306
NM_001018005.2(TPM1):c.284T>C (p.Val95Ala)	rs104894504
NM_001018005.2(TPM1):c.292G>A (p.Glu98Lys)	rs730881131
NM_001018005.2(TPM1):c.337C>G (p.Leu113Val)	rs397516369
NM_001018005.2(TPM1):c.389T>C (p.Ile130Thr)	rs727503517
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.533G>A (p.Arg178His)	rs397516375
NM_001018005.2(TPM1):c.539A>G (p.Glu180Gly)	rs104894502
NM_001018005.2(TPM1):c.574G>A (p.Glu192Lys)	rs199476315
NM_001018005.2(TPM1):c.602C>T (p.Thr201Met)	rs730881141
NM_001018005.2(TPM1):c.688G>A (p.Asp230Asn)	rs199476317
NM_001018005.2(TPM1):c.725C>T (p.Ala242Val)	rs397516387
NM_001018005.2(TPM1):c.742A>G (p.Lys248Glu)	rs199476319

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