Variant #0000126172 (NC_000001.10:g.155264149G>A, NM_000298.5:c.993C>T (PKLR))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.155264149G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PKLR_000048
Frequency 7/13006
Freq. EA 7/8600
Freq. AA 0/4406
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 2013-05-03 19:48:05 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PKLR NM_000298.5 ?/? c.993C>T r.(=) p.(=)