Variant #0000254900 (NC_000012.11:g.133196619A>G, NM_006231.2:c.*4664T>C (POLE))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.133196619A>G
DNA change (hg38) g.132620033A>G
Published as P2RX2(NM_001282165.1):c.491A>G (p.Q164R)
ISCN -
DB-ID P2RX2_000004 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) 0.00071 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +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.*4664T>C r.(=) p.(=)
P2RX2 NM_012226.3 -?/. - c.275A>G r.(?) p.(Gln92Arg)
P2RX2 NM_170682.2 -?/. - c.491A>G r.(?) p.(Gln164Arg)


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