Variant #0000298880 (NC_000001.10:g.155264999C>T, NM_000298.5:c.602G>A (PKLR))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.155264999C>T
DNA change (hg38) g.155295208C>T
Published as PKLR(NM_000298.6):c.602G>A (p.W201*)
ISCN -
DB-ID PKLR_000285
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
PKLR NM_000298.5 +/. - c.602G>A - r.(?) p.(Trp201Ter)
HCN3 NM_020897.2 +/. - c.*6745C>T - r.(=) p.(=)


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