Related gene-specific medical variations for Gene (Select 255119) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3143442	NM_152770.3(CFAP299):c.12A>T (p.Glu4Asp)	CFAP299, LOC129992746 (E4D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1808155	GRCh37/hg19 4q21.21(chr4:81444078-81918621)x1	CFAP299	Copy number loss	not provided	GUncertain significance
Select item 394575	GRCh37/hg19 4q21.21(chr4:81506519-81686491)x1	CFAP299	Copy number loss	See cases	GLikely benign
Select item 152449	GRCh38/hg38 4q21.21(chr4:80772092-80879777)x1	CFAP299	Copy number loss	See cases	GBenign

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