Variant #0000613964 (NC_000012.11:g.133197717G>C, NM_006231.2:c.*3566C>G (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.133197717G>C
DNA change (hg38) g.132621131G>C
Published as P2RX2(NM_001282165.1):c.905G>C (p.R302T)
ISCN -
DB-ID POLE_000201
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POLE NM_006231.2 ?/. - c.*3566C>G r.(=) p.(=)
P2RX2 NM_012226.3 ?/. - c.689G>C r.(?) p.(Arg230Thr)
P2RX2 NM_170682.2 ?/. - c.905G>C r.(?) p.(Arg302Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.