Variant #0000163945 (NC_000021.8:g.34951753T>G, NM_017613.3:c.1466A>C (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.34951753T>G |
| DNA change (hg38) |
g.33579447T>G |
| Published as |
K489T |
| ISCN |
- |
| DB-ID |
DONSON_000003 See all 9 reported entries |
| Variant remarks |
expression cloning showed reduced protein levels, normal subcellular localization (0.9) and did not complement loss of endogenous DONSON by rescuing spontaneous fork stalling after DONSON depletion |
| 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) |
0.001 View details |
| 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 14:16:04 +01:00 (CET) |
| Date last edited |
2020-07-16 22:09:02 +02:00 (CEST) |

Variant on transcripts
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