Variant #0001042146 (NC_000017.10:g.71197816T>C, NM_018714.2:c.1850T>C (COG1))

Chromosome 17
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.71197816T>C
DNA change (hg38) -
Published as COG1(NM_018714.3):c.1850T>C (p.(Leu617Pro))
ISCN -
DB-ID COG1_000052
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG1 NM_018714.2 ?/. - c.1850T>C r.(?) p.(Leu617Pro)
FAM104A NM_032837.2 ?/. - c.*7852A>G r.(=) p.(=)


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