Variant #0000036164 (NC_000009.11:g.132576387C>T, NM_000113.2:c.863G>A (TOR1A))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.132576387C>T
DNA change (hg38) g.129814108C>T
Published as -
ISCN -
DB-ID TOR1A_000004 See all 2 reported entries
Variant remarks expression cloning HEK293 cells reduced expression (0.8), focally enlarged perinuclear space nuclear envelope
Reference PubMed: Zirn 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2014-04-15 20:46:01 +02:00 (CEST)
Date last edited 2025-01-03 14:48:02 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TOR1A NM_000113.2 +/? 5 c.863G>A r.(?) p.Arg288Gln


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