Variant #0000966813 (NC_000012.11:g.133196865dup, NM_006231.2:c.*4418dup (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.133196865dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID POLE_000313
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +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.*4418dup r.(?) p.(=)
P2RX2 NM_012226.3 -?/. - c.351dup r.(?) p.(Thr118Tyrfs*82)
P2RX2 NM_170682.2 -?/. - c.567dup r.(?) p.(Thr190Tyrfs*82)


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