Variant #0000530333 (NC_000007.13:g.107194786del, NM_006348.3:c.330del (COG5))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.107194786del
DNA change (hg38) g.107554341del
Published as COG5(NM_001161520.1):c.330delT (p.V111Lfs*23)
ISCN -
DB-ID DUS4L_000011
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 13:17:13 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR22 NM_005295.2 +/. - c.*78979del r.(?) p.(=)
COG5 NM_006348.3 +/. - c.330del r.(?) p.(Val111LeufsTer23)
HBP1 NM_012257.3 +/. - c.*352910del r.(?) p.(=)
DUS4L NM_181581.2 +/. - c.-9979del r.(?) p.(=)


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