Variant #0000044827 (NC_000016.9:g.3651011G>T, NM_032444.2:c.1132C>A (SLX4))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.3651011G>T |
| DNA change (hg38) |
g.3601010G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SLX4_000075 See all 2 reported entries |
| Variant remarks |
expression cloning Slx4-deficient MEFs mitomycin C resistant |
| Reference |
PubMed: Bakker 2013, Journal: Bakker 2013 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Not applicable |
| 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 |
2012-08-31 16:38:57 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
|