Variant #0000299033 (NC_000012.11:g.133201563G>A, NM_006231.2:c.6675C>T (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.133201563G>A
DNA change (hg38) g.132624977G>A
Published as POLE(NM_006231.3):c.6675C>T (p.R2225=), POLE(NM_006231.4):c.6675C>T (p.R2225=)
ISCN -
DB-ID POLE_000009 See all 4 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) 0.00119 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.6675C>T r.(?) p.(Arg2225=)
P2RX2 NM_012226.3 -?/. - c.*3005G>A r.(=) p.(=)
P2RX2 NM_170682.2 -?/. - c.*3005G>A r.(=) p.(=)


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