List of variants in gene CNOT3 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_014516.4(CNOT3):c.1094C>A (p.Ser365Ter)
NM_014516.4(CNOT3):c.119A>G (p.Gln40Arg)
NM_014516.4(CNOT3):c.1708ATC[1] (p.Ile571del)
NM_014516.4(CNOT3):c.575A>G (p.Asn192Ser)	rs2146595285

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