Variant #0000352571 (NC_000010.10:g.89624263A>G, NM_000314.4:c.37A>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.89624263A>G
DNA change (hg38) g.87864506A>G
Published as K13E
ISCN -
DB-ID PTEN_000324 See all 2 reported entries
Variant remarks expression cloning in yeast and mammalian cells shows no PIP3-phosphatase activity and cytoplasmic location, respectively
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 Rafael Pulido
Date created 2018-02-04 17:31:30 +01:00 (CET)
Date last edited 2022-09-21 08:32:25 +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.37A>G r.(?) p.Lys13Glu


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