"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ZNF839"[ge - 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 2644578	NM_018335.6(ZNF839):c.6G>T (p.Ala2=)	ZNF839	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2644579	NM_018335.6(ZNF839):c.829C>T (p.Leu277=)	ZNF839	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2644580	NM_018335.6(ZNF839):c.1014C>T (p.His338=)	ZNF839	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2644581	NM_018335.6(ZNF839):c.2586C>T (p.Ser862=)	ZNF839	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3024584	GRCh37/hg19 14q32.31(chr14:102749815-103192843)x3	ANKRD9, CINP +4 more	Copy number gain	not provided	GUncertain significance

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File