Variant #0000922964 (NC_000001.10:g.155261709G>A, NM_000298.5:c.1456C>T (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.155261709G>A
DNA change (hg38) -
Published as PKLR(NM_000298.6):c.1456C>T (p.R486W)
ISCN -
DB-ID PKLR_000018 See all 148 reported entries
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) 0.00309 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
PKLR NM_000298.5 +/. - c.1456C>T - r.(?) p.(Arg486Trp)
HCN3 NM_020897.2 +/. - c.*3455G>A - r.(=) p.(=)


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