RGD:150337338 Rat Genome Database

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Variant: RGD:150337338 -  Homo sapiens

RGD ID: 150337338
RS ID: rs253848
ClinVar ID: CV1172383
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PTPRO  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 15,637,336
GRCh38 12 15,484,402
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002848.4:c.349+155C>T
NM_030667.3:c.349+155C>T
NG_031857.1:g.167146C>T
NC_000012.12:g.15484402C>T
More... 		02/03/2020 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PTPRO
Accession:NM_002848
Location:INTRON

Gene Symbol:PTPRO
Accession:NM_030667
Location:INTRON

Gene Symbol:PTPRO
Accession:NM_030669
Location:INTRON

Gene Symbol:PTPRO
Accession:NM_030668
Location:INTRON

Gene Symbol:PTPRO
Accession:NM_030671
Location:INTRON

Gene Symbol:PTPRO
Accession:NM_030670
Location:INTRON

Gene Symbol:PTPRO
Accession:XM_017019725
Location:INTRON

Gene Symbol:PTPRO
Accession:XR_931316
Location:INTRON;NON-CODING

Gene Symbol:PTPRO
Accession:XR_007063106
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001541583 CLINVAR
dbSNP (RS) rs253848 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PTPRO CLINVAR
OMIM 600579 CLINVAR