Variant #0000805615 (NC_000012.11:g.133197699C>T, NM_006231.2:c.*3584G>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.133197699C>T
DNA change (hg38) -
Published as P2RX2(NM_001282165.1):c.887C>T (p.S296L)
ISCN -
DB-ID POLE_000244
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) 4.0E-5 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 2021-09-17 14:40:49 +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.*3584G>A r.(=) p.(=)
P2RX2 NM_012226.3 -?/. - c.671C>T r.(?) p.(Ser224Leu)
P2RX2 NM_170682.2 -?/. - c.887C>T r.(?) p.(Ser296Leu)


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