Variant #0000547156 (NC_000012.11:g.133197899G>A, NM_006231.2:c.*3384C>T (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.133197899G>A
DNA change (hg38) g.132621313G>A
Published as P2RX2(NM_001282165.1):c.964G>A (p.G322R)
ISCN -
DB-ID POLE_000141 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) 0.00024 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.*3384C>T r.(=) p.(=)
P2RX2 NM_012226.3 ?/. - c.748G>A r.(?) p.(Gly250Arg)
P2RX2 NM_170682.2 ?/. - c.964G>A r.(?) p.(Gly322Arg)


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