Variant #0001052784 (NC_000007.13:g.106876963G>A, NM_006348.3:c.2116C>T (COG5))

Chromosome 7
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.106876963G>A
DNA change (hg38) -
Published as COG5(NM_006348.5):c.2023C>T (p.(Arg675Cys))
ISCN -
DB-ID DUS4L_000038
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) 0.00035 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
GPR22 NM_005295.2 ?/. - c.-234885G>A r.(?) p.(=)
COG5 NM_006348.3 ?/. - c.2116C>T r.(?) p.(Arg706Cys)
HBP1 NM_012257.3 ?/. - c.*35087G>A r.(=) p.(=)
DUS4L NM_181581.2 ?/. - c.-327802G>A r.(?) p.(=)


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