Variant #0000610602 (NC_000007.13:g.107188782G>A, NC_000007.13(NM_006348.3):c.386-5C>T (COG5))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.107188782G>A
DNA change (hg38) g.107548337G>A
Published as COG5(NM_001161520.1):c.386-5C>T (p.?)
ISCN -
DB-ID DUS4L_000021
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-23 13:16:54 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPR22 NM_005295.2 -?/. - c.*72975G>A r.(=) p.(=)
COG5 NM_006348.3 -?/. - c.386-5C>T r.spl? p.?
HBP1 NM_012257.3 -?/. - c.*346906G>A r.(=) p.(=)
DUS4L NM_181581.2 -?/. - c.-15983G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.