RGD:11659427 Rat Genome Database

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Variant: RGD:11659427 -  Homo sapiens

RGD ID: 11659427
RS ID: rs886047399
ClinVar ID: CV323706
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PTEN  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 89,725,353
GRCh38 10 87,965,596
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001304718.2:c.*124C>T
LRG_311:g.107158C>T
NG_007466.2:g.107158C>T
NC_000010.11:g.87965596C>T
More... 		01/12/2018 3 prime utr variant uncertain significance PTEN Hamartomatous Tumour Syndrome; PTEN-related disorders
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:PTEN
Accession:NM_001304718
Location:3UTRS;EXON

Gene Symbol:PTEN
Accession:NM_001304717
Location:3UTRS;EXON

Gene Symbol:PTEN
Accession:NM_000314
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000357887 CLINVAR
dbSNP (RS) rs886047399 CLINVAR
MedGen C1959582 CLINVAR
NCBI Gene PTEN CLINVAR
OMIM 601728 CLINVAR