Variant #0000980912 (NC_000014.8:g.50117076dup, NM_002692.3:c.1406dup (POLE2))

Chromosome 14
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.50117076dup
DNA change (hg38) -
Published as POLE2(NM_001348385.1):c.1175dupT (p.L392Ffs*17), POLE2(NM_002692.4):c.1406dupT (p.L469Ffs*17)
ISCN -
DB-ID POLE2_000012 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLE2 NM_002692.3 ?/. - c.1406dup r.(?) p.(Leu469Phefs*17)


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