Variant #0000979497 (NC_000011.9:g.17627514C>T, NM_001277269.1:c.4024C>T (OTOG))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.17627514C>T
DNA change (hg38) -
Published as OTOG(NM_001277269.1):c.4024C>T (p.(Gln1342Ter))
ISCN -
DB-ID OTOG_000189 See all 2 reported entries
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OTOG NM_001277269.1 +?/. - c.4024C>T r.(?) p.(Gln1342*)
OTOG NM_001292063.2 +?/. - c.3988C>T r.(?) p.(Gln1330*)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.