NM_006348.5(COG5):c.1026+17A>G AND COG5-congenital disorder of glycosylation
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003608955.1
Allele description [Variation Report for NM_006348.5(COG5):c.1026+17A>G]
NM_006348.5(COG5):c.1026+17A>G
Condition(s)
- Name:
- COG5-congenital disorder of glycosylation
- Synonyms:
- CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi; Congenital disorder of glycosylation type 2i; CDG IIi; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0013325; MedGen: C3150876; Orphanet: 263487; OMIM: 613612
-
-10 eggc.vipjXB (3107)
BioProject
-
Leukotriene B4 effect on monocytes: time course
Leukotriene B4 effect on monocytes: time courseAccession: GDS3088GEO DataSets
-
Related DataSets for GEO Profiles (Select 48313924) (1)
GEO DataSets
-
Mus musculus adult female vagina cDNA, RIKEN full-length enriched library, clone...
Mus musculus adult female vagina cDNA, RIKEN full-length enriched library, clone:9930021D14 product:hypothetical Haem peroxidase superfamily containing protein, full insert sequencegi|26347990|dbj|AK079437.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Feb 28, 2024