Variant #0000126153 (NC_000001.10:g.155263079C>T, NM_000298.5:c.1325G>A (PKLR))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.155263079C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PKLR_000057
Frequency 1/13006
Freq. EA 0/8600
Freq. AA 1/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:20:35 +02:00 (CEST)
Date last edited 2024-12-06 02:56:02 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PKLR NM_000298.5 ?/? c.1325G>A r.(?) p.(Arg442His)