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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

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


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