Variant #0000547159 (NC_000012.11:g.133198474T>A, NM_006231.2:c.*2809A>T (POLE))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.133198474T>A
DNA change (hg38) g.132621888T>A
Published as P2RX2(NM_170683.3):c.1410T>A (p.P470=)
ISCN -
DB-ID POLE_000144
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 2019-07-18 18:22:55 +02:00 (CEST)
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.*2809A>T r.(=) p.(=)
P2RX2 NM_012226.3 -/. - c.1116T>A r.(?) p.(Pro372=)
P2RX2 NM_170682.2 -/. - c.1332T>A r.(?) p.(Pro444=)


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