Variant #0000443384 (NC_000006.11:g.123892124G>C, NM_006073.3:c.176C>G (TRDN))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.123892124G>C
DNA change (hg38) g.123570979G>C
Published as -
ISCN -
DB-ID TRDN_000002 See all 4 reported entries
Variant remarks in vivo mouse expression cloning, cardiomyocytes normal transcript stability, WB/IHC no TRDN protein
Reference PubMed: Roux-Buisson 2012
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-05-24 22:08:34 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRDN NM_006073.3 +/. 2 c.176C>G r.(?) p.Thr59Arg


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