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 International |
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) |

Variant on transcripts
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