List of variants in gene ACTG1 reported as uncertain significance for not specified

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001614.5(ACTG1):c.-1A>G	rs781801921	0.00008
NM_001614.5(ACTG1):c.*11C>T	rs782341016	0.00002
NM_001614.5(ACTG1):c.519C>T (p.His173=)	rs781859294	0.00001
NM_001614.5(ACTG1):c.1036C>G (p.Leu346Val)	rs782217473
NM_001614.5(ACTG1):c.1039G>T (p.Ala347Ser)	rs1555666373
NM_001614.5(ACTG1):c.1051A>C (p.Thr351Pro)	rs727502880
NM_001614.5(ACTG1):c.270C>A (p.Phe90Leu)
NM_001614.5(ACTG1):c.377C>T (p.Thr126Ile)	rs876657740
NM_001614.5(ACTG1):c.409C>G (p.Gln137Glu)	rs876657741
NM_001614.5(ACTG1):c.521C>G (p.Ala174Gly)	rs727504862
NM_001614.5(ACTG1):c.548G>A (p.Arg183Gln)	rs781945750
NM_001614.5(ACTG1):c.853T>C (p.Cys285Arg)	rs727502882
NM_001614.5(ACTG1):c.985-5dup	rs782289893

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