Variant #0000436080 (NC_000007.13:g.157160096T>A, NM_058246.3:c.265T>A (DNAJB6))
Chromosome |
7 |
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.157160096T>A |
DNA change (hg38) |
g.157367402T>A |
Published as |
267T>A |
ISCN |
- |
DB-ID |
DNAJB6_000002 See all 32 reported entries |
Variant remarks |
expression cloning with pEGFP/HD-120Q significantly impaired anti-aggregation function |
Reference |
PubMed: Sarparanta 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 |
2012-04-02 22:51:22 +02:00 (CEST) |
Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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