Variant #0001038378 (NC_000011.9:g.17582640C>T, NM_001277269.1:c.1490C>T (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.17582640C>T
DNA change (hg38) -
Published as OTOG(NM_001292063.2):c.1454C>T (p.(Thr485Ile))
ISCN -
DB-ID OTOG_000201
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_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     
OTOG NM_001277269.1 ?/. - c.1490C>T r.(?) p.(Thr497Ile)
OTOG NM_001292063.2 ?/. - c.1454C>T r.(?) p.(Thr485Ile)


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