"PreventionGenetics, part of Exact Sciences"[submitter] AND "CFAP69"[g - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058348	NM_001039706.3(CFAP69):c.-7A>C	CFAP69	Single nucleotide variant (5 prime UTR variant)	CFAP69-related condition	GLikely benign
Select item 768178	NM_001039706.3(CFAP69):c.36C>T (p.Ala12=)	CFAP69	Single nucleotide variant (synonymous variant)	CFAP69-related condition +1 more	GBenign
Select item 3044692	NM_001039706.3(CFAP69):c.136A>G (p.Met46Val)	CFAP69 (M46V)	Single nucleotide variant (missense variant)	CFAP69-related condition	GLikely benign
Select item 712004	NM_001039706.3(CFAP69):c.317G>A (p.Arg106His)	CFAP69 (R106H)	Single nucleotide variant (missense variant)	CFAP69-related condition +1 more	GBenign
Select item 768179	NM_001039706.3(CFAP69):c.916C>T (p.Arg306Cys)	CFAP69 (R288C +1 more)	Single nucleotide variant (missense variant)	CFAP69-related condition +1 more	GBenign
Select item 3060732	NM_001039706.3(CFAP69):c.1116C>T (p.Asn372=)	CFAP69	Single nucleotide variant (synonymous variant)	CFAP69-related condition	GBenign
Select item 1192635	NM_001039706.3(CFAP69):c.1468G>A (p.Val490Met)	CFAP69 (V472M +1 more)	Single nucleotide variant (missense variant)	CFAP69-related condition +1 more	GBenign
Select item 3049257	NM_001039706.3(CFAP69):c.1623A>G (p.Leu541=)	CFAP69	Single nucleotide variant (synonymous variant)	CFAP69-related condition	GLikely benign
Select item 712005	NM_001039706.3(CFAP69):c.1686C>T (p.Ile562=)	CFAP69	Single nucleotide variant (synonymous variant)	CFAP69-related condition +1 more	GBenign
Select item 1192637	NM_001039706.3(CFAP69):c.2562C>G (p.Ser854Arg)	CFAP69 (S788R +2 more)	Single nucleotide variant (missense variant)	CFAP69-related condition +1 more	GBenign
Select item 1192638	NM_001039706.3(CFAP69):c.2654C>T (p.Thr885Met)	CFAP69 (T819M +2 more)	Single nucleotide variant (missense variant)	CFAP69-related condition +1 more	GBenign
Select item 3055039	NM_001039706.3(CFAP69):c.2681T>G (p.Val894Gly)	CFAP69 (V828G +2 more)	Single nucleotide variant (missense variant)	CFAP69-related condition	GLikely benign