Variant #0000726651 (NC_000017.10:g.71202892dup, NM_018714.2:c.2665dup (COG1))

Chromosome 17
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.71202892dup
DNA change (hg38) -
Published as COG1(NM_018714.3):c.2665dupC (p.R889Pfs*12)
ISCN -
DB-ID COG1_000030
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG1 NM_018714.2 +/. - c.2665dup r.(?) p.(Arg889Profs*12)
FAM104A NM_032837.2 +/. - c.*2781dup r.(?) p.(=)


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