Variant #0000578993 (NC_000001.10:g.155271434del, NM_000298.5:- (PKLR))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.155271434del |
DNA change (hg38) |
g.155301643del |
Published as |
-248delT |
ISCN |
- |
DB-ID |
PKLR_000074 See all 6 reported entries |
Variant remarks |
in vitro expression K562 cells shows significant increased promoter activity |
Reference |
PubMed: Van Wijk 2003 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Richard van Wijk |
Database submission license |
No license selected |
Created by |
Richard van Wijk |
Date created |
2012-12-18 15:11:00 +01:00 (CET) |
Date last edited |
2022-02-19 12:39:09 +01:00 (CET) |

Variant on transcripts
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