Variant #0000248701 (NC_000017.10:g.71192873A>G, NM_018714.2:c.543A>G (COG1))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71192873A>G
DNA change (hg38) g.73196734A>G
Published as COG1(NM_018714.3):c.543A>G (p.A181=)
ISCN -
DB-ID COG1_000004
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) 0.50028 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 2018-01-15 20:58:59 +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     
COG1 NM_018714.2 -/. - c.543A>G r.(?) p.(Ala181=)
FAM104A NM_032837.2 -/. - c.*12795T>C r.(=) p.(=)


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