Variant #0000852849 (NC_000011.9:g.17660080C>G, NM_001277269.1:c.7914C>G (OTOG))

Chromosome 11
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.17660080C>G
DNA change (hg38) -
Published as OTOG(NM_001277269.1):c.7914C>G (p.C2638W)
ISCN -
DB-ID OTOG_000183
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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OTOG NM_001277269.1 ?/. - c.7914C>G r.(?) p.(Cys2638Trp)
OTOG NM_001292063.2 ?/. - c.7878C>G r.(?) p.(Cys2626Trp)


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