Variant #0000613966 (NC_000012.11:g.133201579_133201594dup, NC_000012.11(NM_006231.2):c.6658-10_6663dup (POLE))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.133201579_133201594dup
DNA change (hg38) g.132624993_132625008dup
Published as -
ISCN -
DB-ID POLE_000203
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLE NM_006231.2 ?/. - c.6658-10_6663dup r.spl? p.?
P2RX2 NM_012226.3 ?/. - c.*3021_*3036dup r.(=) p.(=)
P2RX2 NM_170682.2 ?/. - c.*3021_*3036dup r.(=) p.(=)


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