Variant #0001026753 (NC_000016.9:g.70513133A>C, NM_015386.2:c.*1780T>G (COG4))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.70513133A>C
DNA change (hg38) -
Published as FCSK(NM_145059.3):c.2980A>C (p.K994Q)
ISCN -
DB-ID FUK_000024
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) 0.00023 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 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG4 NM_015386.2 ?/. - c.*1780T>G r.(=) p.(=)
FUK NM_145059.2 ?/. - c.2980A>C r.(?) p.(Lys994Gln)


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