Variant #0001041287 (NC_000016.9:g.69363024G>A, NM_032382.4:c.*85C>T (COG8))

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.69363024G>A
DNA change (hg38) -
Published as COG8(NM_001379266.1):c.1472C>T (p.(Ser491Leu))
ISCN -
DB-ID COG8_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) 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VPS4A NM_013245.2 ?/. - c.*4812G>A r.(=) p.(=)
NIP7 NM_016101.4 ?/. - c.-10709G>A r.(?) p.(=)
PDF NM_022341.1 ?/. - c.633C>T r.(?) p.(=)
COG8 NM_032382.4 ?/. - c.*85C>T r.(=) p.(=)


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