Variant #0001036049 (NC_000007.13:g.106938586_106938591del, NC_000007.13(NM_006348.3):c.1406_1406+5del (COG5))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.106938586_106938591del
DNA change (hg38) -
Published as COG5(NM_006348.5):c.1313_1313+5del
ISCN -
DB-ID DUS4L_000037
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     
GPR22 NM_005295.2 +?/. - c.-173262_-173257del r.(?) p.(=)
COG5 NM_006348.3 +?/. - c.1406_1406+5del r.(?) p.(Tyr468_Asp469del)
HBP1 NM_012257.3 +?/. - c.*96710_*96715del r.(=) p.(=)
DUS4L NM_181581.2 +?/. - c.-266179_-266174del r.(?) p.(=)


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