"PreventionGenetics, part of Exact Sciences"[submitter] AND "CCNF"[gen - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043448	NM_001761.3(CCNF):c.220G>A (p.Ala74Thr)	CCNF (A74T)	Single nucleotide variant (missense variant +1 more)	CCNF-related condition	GBenign
Select item 3044799	NM_001761.3(CCNF):c.347-4G>A	CCNF	Single nucleotide variant (intron variant)	CCNF-related condition	GLikely benign
Select item 3034783	NM_001761.3(CCNF):c.435C>T (p.Ala145=)	CCNF	Single nucleotide variant (5 prime UTR variant +1 more)	CCNF-related condition	GLikely benign
Select item 748643	NM_001761.3(CCNF):c.540+3G>A	CCNF	Single nucleotide variant (intron variant)	CCNF-related condition +1 more	GLikely benign
Select item 3051951	NM_001761.3(CCNF):c.1047G>T (p.Arg349=)	CCNF	Single nucleotide variant (synonymous variant)	CCNF-related condition	GLikely benign
Select item 3044570	NM_001761.3(CCNF):c.1056C>T (p.Leu352=)	CCNF	Single nucleotide variant (synonymous variant)	CCNF-related condition	GLikely benign
Select item 775366	NM_001761.3(CCNF):c.1188G>T (p.Glu396Asp)	CCNF (E88D +1 more)	Single nucleotide variant (missense variant)	CCNF-related condition +1 more	GBenign/Likely benign
Select item 3047555	NM_001761.3(CCNF):c.1233G>A (p.Val411=)	CCNF	Single nucleotide variant (synonymous variant)	CCNF-related condition	GLikely benign
Select item 3035972	NM_001761.3(CCNF):c.1592T>G (p.Leu531Arg)	CCNF (L223R +1 more)	Single nucleotide variant (missense variant)	CCNF-related condition	GLikely benign
Select item 722268	NM_001761.3(CCNF):c.2072G>A (p.Arg691Gln)	CCNF, LOC105371050 (R383Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3039769	NM_001761.3(CCNF):c.2112C>T (p.Ser704=)	CCNF, LOC105371050	Single nucleotide variant (synonymous variant)	CCNF-related condition	GLikely benign