Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

ClinVar Genomic variation as it relates to human health

Advanced search

NM_018714.3(COG1):c.1480A>G (p.Asn494Asp)

Help
Interpretation:
Uncertain significance​

Review status:
criteria provided, single submitter
Submissions:
1
First in ClinVar:
May 31, 2020
Most recent Submission:
May 31, 2020
Last evaluated:
Jan 12, 2018
Accession:
VCV000891220.2
Variation ID:
891220
Description:
single nucleotide variant
Help

NM_018714.3(COG1):c.1480A>G (p.Asn494Asp)

Allele ID
878342
Variant type
single nucleotide variant
Variant length
1 bp
Cytogenetic location
17q25.1
Genomic location
17: 73201307 (GRCh38) GRCh38 UCSC
17: 71197446 (GRCh37) GRCh37 UCSC
HGVS
Nucleotide Protein Molecular
consequence
NM_018714.3:c.1480A>G MANE Select NP_061184.1:p.Asn494Asp missense
NC_000017.11:g.73201307A>G
NC_000017.10:g.71197446A>G
NG_008971.1:g.13274A>G
Protein change
N494D
Other names
-
Canonical SPDI
NC_000017.11:73201306:A:G
Functional consequence
-
Global minor allele frequency (GMAF)
-

Allele frequency
The Genome Aggregation Database (gnomAD) 0.00001
Trans-Omics for Precision Medicine (TOPMed) 0.00001
Exome Aggregation Consortium (ExAC) 0.00007
Trans-Omics for Precision Medicine (TOPMed) 0.00002
The Genome Aggregation Database (gnomAD), exomes 0.00005
Links
dbSNP: rs779677895
VarSome
Help

Aggregate interpretations per condition

Interpreted condition Interpretation Number of submissions Review status Last evaluated Variation/condition record
Uncertain significance 1 criteria provided, single submitter Jan 12, 2018 RCV001126371.2
Help
Gene OMIM ClinGen Gene Dosage Sensitivity Curation Variation viewer Related variants
HI score Help TS score Help Within gene All
COG1 - - GRCh38
GRCh37
241 278

Submitted interpretations and evidence

Help
Interpretation
(Last evaluated)
Review status
(Assertion criteria)
Condition
(Inheritance)
Submitter More information
Uncertain significance
(Jan 12, 2018)
criteria provided, single submitter
Method: clinical testing
COG1 congenital disorder of glycosylation
Affected status: unknown
Allele origin: germline
Illumina Laboratory Services,Illumina
Accession: SCV001285554.1
First in ClinVar: May 31, 2020
Last updated: May 31, 2020
Comment:
This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated … (more)

Functional evidence

Help
There is no functional evidence in ClinVar for this variation. If you have generated functional data for this variation, please consider submitting that data to ClinVar.

Citations for this variant

Help
There are no citations in ClinVar for this variation. If you know of citations for this variation, please consider submitting that information to ClinVar.

Text-mined citations for rs779677895...

Help
These citations are identified by LitVar using the rs number, so they may include citations for more than one variant at this location. Please review the LitVar results carefully for your variant of interest.

Record last updated Apr 25, 2022