RGD:13509798 Rat Genome Database

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Variant: RGD:13509798 -  Homo sapiens

RGD ID: 13509798
RS ID: rs1036616021
ClinVar ID: CV481956
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC130004273  PTEN  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 89,623,443
GRCh38 10 87,863,686
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000010.10:g.89623443G>T
LRG_311:g.5249G>T
NC_000010.11:g.87863686G>T
NG_007466.2:g.5249G>T
More... 		07/01/2016 5 prime utr variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:PTEN
Accession:NM_000314
Location:5UTRS;EXON

Gene Symbol:PTEN
Accession:NM_001304718
Location:5UTRS;EXON

Gene Symbol:PTEN
Accession:NM_001304717
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000587779 CLINVAR
dbSNP (RS) rs1036616021 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene LOC130004273 CLINVAR
  PTEN CLINVAR
OMIM 601728 CLINVAR