"CCNO-related condition"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File

Search results

Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 696778	NM_021147.5(CCNO):c.999C>T (p.His333=)	CCNO	Single nucleotide variant (synonymous variant +1 more)	CCNO-related condition +1 more	GLikely benign
Select item 411598	NM_021147.5(CCNO):c.788G>C (p.Arg263Pro)	CCNO (R263P)	Single nucleotide variant (missense variant +1 more)	CCNO-related condition +1 more	GUncertain significance
Select item 411595	NM_021147.5(CCNO):c.685G>A (p.Gly229Ser)	CCNO (G229S)	Single nucleotide variant (missense variant +1 more)	CCNO-related condition +1 more	GUncertain significance
Select item 416792	NM_021147.5(CCNO):c.354G>A (p.Pro118=)	CCNO	Single nucleotide variant (synonymous variant +1 more)	CCNO-related condition +1 more	GBenign/Likely benign
Select item 857554	NM_021147.5(CCNO):c.16C>A (p.Pro6Thr)	CCNO (P6T)	Single nucleotide variant (missense variant +1 more)	CCNO-related condition +1 more	GUncertain significance

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File