Variant #0000621795 (NC_000007.13:g.107198449C>T, NM_006348.3:c.299G>A (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.107198449C>T
DNA change (hg38) g.107558004C>T
Published as COG5(NM_001161520.2):c.206G>A (p.S69N)
ISCN -
DB-ID DUS4L_000022
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*82642C>T r.(=) p.(=)
COG5 NM_006348.3 ?/. - c.299G>A r.(?) p.(Ser100Asn)
HBP1 NM_012257.3 ?/. - c.*356573C>T r.(=) p.(=)
DUS4L NM_181581.2 ?/. - c.-6316C>T r.(?) p.(=)


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