Variant #0000808237 (NC_000017.10:g.71192766C>T, NM_018714.2:c.436C>T (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.71192766C>T
DNA change (hg38) -
Published as COG1(NM_018714.2):c.436C>T (p.L146F)
ISCN -
DB-ID COG1_000033
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COG1 NM_018714.2 ?/. - c.436C>T r.(?) p.(Leu146Phe)
FAM104A NM_032837.2 ?/. - c.*12902G>A r.(=) p.(=)


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