List of variants in gene TPM1 reported as not provided for not provided

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_001018005.2(TPM1):c.453C>A (p.Ala151=)	rs1071646	0.64628
NM_001018005.2(TPM1):c.486T>C (p.Tyr162=)	rs11558747	0.05001
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.850A>G (p.Ile284Val)	rs199476322	0.00001
NM_001018005.2(TPM1):c.109A>G (p.Lys37Glu)	rs199476303
NM_001018005.2(TPM1):c.172G>C (p.Asp58His)	rs199476304
NM_001018005.2(TPM1):c.184G>C (p.Glu62Gln)	rs199476305
NM_001018005.2(TPM1):c.188C>T (p.Ala63Val)	rs199476306
NM_001018005.2(TPM1):c.209A>C (p.Lys70Thr)	rs199476307
NM_001018005.2(TPM1):c.241-12_241-11delinsTG	rs199476309
NM_001018005.2(TPM1):c.275T>C (p.Ile92Thr)	rs199476310
NM_001018005.2(TPM1):c.403C>A (p.Gln135Lys)	rs11558749
NM_001018005.2(TPM1):c.45G>T (p.Lys15Asn)	rs199476301
NM_001018005.2(TPM1):c.479G>A (p.Arg160His)	rs199476311
NM_001018005.2(TPM1):c.515T>C (p.Ile172Thr)	rs199476312
NM_001018005.2(TPM1):c.539A>T (p.Glu180Val)	rs104894502
NM_001018005.2(TPM1):c.549T>G (p.Ala183=)	rs199476313
NM_001018005.2(TPM1):c.554T>G (p.Leu185Arg)	rs199476314
NM_001018005.2(TPM1):c.574G>A (p.Glu192Lys)	rs199476315
NM_001018005.2(TPM1):c.61= (p.Arg21=)	rs1437698471
NM_001018005.2(TPM1):c.67G>C (p.Glu23Gln)	rs199476302
NM_001018005.2(TPM1):c.688G>A (p.Asp230Asn)	rs199476317
NM_001018005.2(TPM1):c.715G>A (p.Ala239Thr)	rs199476318
NM_001018005.2(TPM1):c.742A>G (p.Lys248Glu)	rs199476319
NM_001018005.2(TPM1):c.830C>T (p.Ala277Val)	rs199476320

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