Variant #0000266873 (NC_000016.9:g.70515355C>T, NM_015386.2:c.2142G>A (COG4))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.70515355C>T
DNA change (hg38) g.70481452C>T
Published as COG4(NM_015386.3):c.2142G>A (p.S714=)
ISCN -
DB-ID COG4_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.41601 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG4 NM_015386.2 -/. - c.2142G>A r.(?) p.(Ser714=)
FUK NM_145059.2 -/. - c.*1772C>T r.(=) p.(=)


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