List of variants in gene ACTG1 reported as benign by Athena Diagnostics Inc

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001614.5(ACTG1):c.1026T>C (p.Gly342=)	rs1139406	0.04214
NM_001614.5(ACTG1):c.1014G>A (p.Ser338=)	rs1139807	0.04188
NM_001614.5(ACTG1):c.1128A>G (p.Ter376=)	rs11549223	0.04188
NM_001614.5(ACTG1):c.399C>T (p.Tyr133=)	rs2230158	0.01567
NM_001614.5(ACTG1):c.729C>T (p.Pro243=)	rs2230159	0.01563
NM_001614.5(ACTG1):c.177G>A (p.Gln59=)	rs11549220	0.01161
NM_001614.5(ACTG1):c.714G>A (p.Lys238=)	rs11549173	0.00287
NM_001614.5(ACTG1):c.774G>A (p.Pro258=)	rs61997068	0.00053
NM_001614.5(ACTG1):c.126C>T (p.Gly42=)	rs11549197	0.00029
NM_001614.5(ACTG1):c.558C>T (p.Thr186=)	rs142893042

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