Variant #0000724775 (NC_000014.8:g.50154857C>T, NM_002692.3:c.65G>A (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.50154857C>T
DNA change (hg38) -
Published as POLE2(NM_002692.4):c.65G>A (p.R22H)
ISCN -
DB-ID KLHDC1_000002
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 2021-02-08 18:36:18 +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)     

RNA change     

Protein     
POLE2 NM_002692.3 ?/. - c.65G>A r.(?) p.(Arg22His)
KLHDC1 NM_172193.2 ?/. - c.-5056C>T r.(?) p.(=)


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