Variant #0000351723 (NC_000010.10:g.89624275C>A, NM_000314.4:c.49C>G (PTEN))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.89624275C>A
DNA change (hg38) -
Published as Q17E
ISCN -
DB-ID PTEN_000162 See all 2 reported entries
Variant remarks expression cloning in yeast and mammalian cells shows partial PIP3-phosphatase activity, nuclear location
Reference PubMed: Mingo 2018
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rafael Pulido
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2018-02-01 16:00:07 +01:00 (CET)
Date last edited 2022-09-21 08:32:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTEN NM_000314.4 +/. 1 c.49C>G - p.Gln17Glu


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