Variant #0000001584 (NC_000010.11:g.87933129T>A, NM_000314.6:c.370T>A (PTEN))

Individual ID 00000340
Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.87933129T>A
Published as -
Reference Jafri Malin Abdullah et al. (2006), dbSNP, ClinVar
DB-ID PTEN_000005 See all 2 reported entries
dbSNP ID rs121909223
Frequency 1/37
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-10 14:49:35 +08:00 (CST)
Date last edited 2021-09-01 15:09:46 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
PTEN NM_000314.6 +?/. 5 c.370T>A - r.(?) p.(Cys124Ser) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000355 DNA PCR;SSCA PTEN 6 Nuur Athirah Binti Mohd Daud