Variant #0000840749 (NC_000001.10:g.155271274A>C, 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.155271274A>C
DNA change (hg38) g.155301483A>C
Published as c.-88T>G
ISCN -
DB-ID PKLR_000062 See all 26 reported entries
Variant remarks in vitro expression K562 cells shows increased promoter activity (1.5)
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 Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-02-19 13:40:56 +01:00 (CET)
Date last edited 2025-02-27 08:35:17 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
PKLR NM_000298.5 +/. _1 - - r.=|inc p.=|inc


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.