List of variants in gene TPM1 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001018005.1(TPM1):c.-106C>T	rs886051320	0.00016
NM_001018005.2(TPM1):c.829G>A (p.Ala277Thr)	rs149659674	0.00009
NM_001018005.1(TPM1):c.-114G>A	rs886051319	0.00004
NM_001018005.2(TPM1):c.-7C>A	rs370871307	0.00001
NM_001018005.2(TPM1):c.114+3C>T	rs112677344	0.00001
NM_001018005.2(TPM1):c.115-5C>G	rs753196985	0.00001
NM_001018005.2(TPM1):c.118G>T (p.Glu40Ter)	rs104894501	0.00001
NM_001018005.2(TPM1):c.272G>A (p.Arg91His)	rs1477561695	0.00001
NM_001018005.2(TPM1):c.314G>A (p.Arg105His)	rs773149185	0.00001
NM_001018005.2(TPM1):c.511A>G (p.Ile171Val)	rs774903903	0.00001
NM_001018005.2(TPM1):c.630G>T (p.Gln210His)	rs761816813	0.00001
NM_001018005.2(TPM1):c.1A>G (p.Met1Val)	rs367543668
NM_001018005.2(TPM1):c.252C>G (p.Asp84Glu)	rs369617788
NM_001018005.2(TPM1):c.262C>G (p.Leu88Val)	rs1555407795
NM_001018005.2(TPM1):c.2T>C (p.Met1Thr)	rs1475635564
NM_001018005.2(TPM1):c.563+249C>T	rs397516379

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