Variant #0001030035 (NC_000010.10:g.89692905G>A, NM_000314.4:c.389G>A (PTEN))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89692905G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PTEN_000019 See all 7 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs121909229
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-24 17:01:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTEN NM_000314.4 +/. - c.389G>A r.(?) p.(Arg130Gln)


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