Variant #0000914962 (NC_000017.10:g.71199822C>G, NM_018714.2:c.2272C>G (COG1))

Chromosome 17
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.71199822C>G
DNA change (hg38) -
Published as COG1(NM_018714.2):c.2272C>G (p.(Arg758Gly))
ISCN -
DB-ID COG1_000042
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 2023-01-11 15:44:22 +01:00 (CET)
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.2272C>G r.(?) p.(Arg758Gly)
FAM104A NM_032837.2 -?/. - c.*5846G>C r.(=) p.(=)


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