RGD:150543235 Rat Genome Database

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Variant: RGD:150543235 -  Homo sapiens

RGD ID: 150543235
RS ID: rs75229593
ClinVar ID: CV1308911
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126861467  PTPRO  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 15,678,835
GRCh38 12 15,525,901
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_030667.3:c.2044-241A>C
NC_000012.12:g.15525901A>C
NC_000012.11:g.15678835A>C
NM_002848.4:c.2044-241A>C
More... 		11/02/2020 intron variant likely benign none provided

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

Gene Symbol:PTPRO
Accession:NM_030670
Location:INTRON

Gene Symbol:PTPRO
Accession:NM_030667
Location:INTRON

Gene Symbol:PTPRO
Accession:NM_030671
Location:INTRON

Gene Symbol:PTPRO
Accession:NM_030669
Location:INTRON

Gene Symbol:PTPRO
Accession:XM_017019725
Location:INTRON

Gene Symbol:PTPRO
Accession:NM_030668
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 RCV001769824 CLINVAR
dbSNP (RS) rs75229593 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126861467 CLINVAR
  PTPRO CLINVAR
OMIM 600579 CLINVAR