Variant #0001039107 (NC_000012.11:g.133263900A>G, NM_006231.2:c.2T>C (POLE))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.133263900A>G
DNA change (hg38) -
Published as POLE(NM_006231.4):c.2T>C (p.(Met1?))
ISCN -
DB-ID POLE_000358
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
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.2T>C r.(?) p.?
PXMP2 NM_018663.1 +?/. - c.-357A>G r.(?) p.(=)


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