RGD:150471814 Rat Genome Database

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Variant: RGD:150471814 -  Homo sapiens

RGD ID: 150471814
RS ID: rs10732674
ClinVar ID: CV1259190
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124902975  PTPRQ  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 80,899,644
GRCh38 12 80,505,865
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001145026.2:c.2273-159G>A
NG_034052.1:g.66520G>A
NC_000012.12:g.80505865G>A
NC_000012.11:g.80899644G>A
 11/12/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PTPRQ
Accession:NM_001145026
Location:INTRON

Gene Symbol:LOC124902975
Accession:XR_007063389
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001684435 CLINVAR
dbSNP (RS) rs10732674 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PTPRQ CLINVAR
OMIM 603317 CLINVAR