RGD:150413260 Rat Genome Database

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Variant: RGD:150413260 -  Homo sapiens

RGD ID: 150413260
RS ID: rs140858403
ClinVar ID: CV1197212
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126807011  RBPJ  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 4 26,408,095
GRCh38 4 26,406,473
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001379409.1:c.149+203A>G
NM_001374401.1:c.152+203A>G
NM_001374402.1:c.152+203A>G
NM_001379407.1:c.152+203A>G
More... 		06/28/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RBPJ
Accession:NM_001379406
Location:INTRON

Gene Symbol:RBPJ
Accession:XM_047415656
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_001374402
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_001379408
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_001379407
Location:INTRON

Gene Symbol:RBPJ
Accession:XM_017008171
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_001374401
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_001379409
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_203284
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_001374403
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_005349
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_015874
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_203283
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_001363577
Location:INTRON

Gene Symbol:RBPJ
Accession:XM_011513840
Location:INTRON

Gene Symbol:RBPJ
Accession:NM_001374400
Location:INTRON

Gene Symbol:RBPJ
Accession:XM_047415657
Location:INTRON

Gene Symbol:RBPJ
Accession:XM_047415658
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001574565 CLINVAR
dbSNP (RS) rs140858403 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126807011 CLINVAR
  RBPJ CLINVAR
OMIM 147183 CLINVAR