Variant #0000163950 (NC_000021.8:g.34950684_34950686dup, NM_017613.3:c.1628_1630dup (DONSON))
Chromosome |
21 |
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.34950684_34950686dup |
DNA change (hg38) |
g.33578378_33578380dup |
Published as |
Q543_I544insK |
ISCN |
- |
DB-ID |
DONSON_000008 See all 3 reported entries |
Variant remarks |
expression cloning showed disrupted subcellular localization (0.3) |
Reference |
PubMed: Reynolds 2017, Journal: Reynolds 2017 |
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 |
2017-03-17 14:33:43 +01:00 (CET) |
Date last edited |
2020-07-16 22:08:53 +02:00 (CEST) |

Variant on transcripts
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