Variant #0000300888 (NC_000001.10:g.155260383G>T, NM_000298.5:c.1705C>A (PKLR))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.155260383G>T
DNA change (hg38) g.155290592G>T
Published as PKLR(NM_000298.6):c.1705C>A (p.R569=)
ISCN -
DB-ID PKLR_000247 See all 2 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) 0.33581 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.1705C>A - r.(?) p.(Arg569=)
HCN3 NM_020897.2 -/. - c.*2129G>T - r.(=) p.(=)


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