List of variants in gene ACTG1 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001614.5(ACTG1):c.1003C>T (p.Arg335Cys)	rs1568060200
NM_001614.5(ACTG1):c.1036C>G (p.Leu346Val)	rs782217473
NM_001614.5(ACTG1):c.131T>A (p.Met44Lys)	rs886041280
NM_001614.5(ACTG1):c.197C>T (p.Thr66Ile)
NM_001614.5(ACTG1):c.277G>A (p.Glu93Lys)	rs1568062529
NM_001614.5(ACTG1):c.547C>T (p.Arg183Trp)	rs1362994447
NM_001614.5(ACTG1):c.611C>G (p.Ala204Gly)	rs11549225
NM_001614.5(ACTG1):c.616C>T (p.Arg206Trp)	rs1598548614
NM_001614.5(ACTG1):c.637A>C (p.Lys213Gln)	rs1057524703
NM_001614.5(ACTG1):c.721G>A (p.Glu241Lys)	rs267606631
NM_001614.5(ACTG1):c.760C>T (p.Arg254Trp)	rs281875328
NM_001614.5(ACTG1):c.761_781dup (p.Arg254_Ala260dup)	rs2143776740
NM_001614.5(ACTG1):c.824A>T (p.His275Leu)	rs2143775813
NM_001614.5(ACTG1):c.847A>G (p.Met283Val)	rs1555666509
NM_001614.5(ACTG1):c.863A>G (p.Asp288Gly)	rs886041756

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