Variant #0000890408 (NC_000012.11:g.133198395C>T, NM_006231.2:c.*2888G>A (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.133198395C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID POLE_000276
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 2022-11-01 13:01:21 +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.*2888G>A r.(=) p.(=)
P2RX2 NM_012226.3 -?/. - c.1037C>T r.(?) p.(Pro346Leu)
P2RX2 NM_170682.2 -?/. - c.1253C>T r.(?) p.(Pro418Leu)


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