Variant #0001026140 (NC_000012.11:g.133253974C>T, NM_006231.2:c.776G>A (POLE))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.133253974C>T
DNA change (hg38) -
Published as POLE(NM_006231.2):c.776G>A (p.(Arg259His)), POLE(NM_006231.3):c.776G>A (p.R259H), POLE(NM_006231.4):c.776G>A (p.R259H)
ISCN -
DB-ID POLE_000093 See all 6 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) 0.00519 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 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLE NM_006231.2 -?/. - c.776G>A r.(?) p.(Arg259His)


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