Variant #0001041300 (NC_000016.9:g.70512256T>C, NM_015386.2:c.*2657A>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.70512256T>C
DNA change (hg38) -
Published as FCSK(NM_145059.3):c.2723T>C (p.(Val908Ala))
ISCN -
DB-ID FUK_000026
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG4 NM_015386.2 ?/. - c.*2657A>G r.(=) p.(=)
FUK NM_145059.2 ?/. - c.2723T>C r.(?) p.(Val908Ala)


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