RGD:15173187 Rat Genome Database

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Variant: RGD:15173187 -  Homo sapiens

RGD ID: 15173187
RS ID: rs199689769
ClinVar ID: CV777886
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRP1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 33,469,296
GRCh38 10 33,180,368
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001244972.2:c.2465-3T>C
NM_003873.7:c.2483-3T>C
NM_001330068.2:c.2432-3T>C
NM_001244973.2:c.2462-3T>C
More... 		12/31/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NRP1
Accession:XM_047425976
Location:INTRON

Gene Symbol:NRP1
Accession:NM_001330068
Location:INTRON

Gene Symbol:NRP1
Accession:NM_003873
Location:INTRON

Gene Symbol:NRP1
Accession:NM_001244973
Location:INTRON

Gene Symbol:NRP1
Accession:XM_006717522
Location:INTRON

Gene Symbol:NRP1
Accession:NM_001024628
Location:INTRON

Gene Symbol:NRP1
Accession:XM_017016865
Location:INTRON

Gene Symbol:NRP1
Accession:NM_001024629
Location:INTRON

Gene Symbol:NRP1
Accession:XM_011519756
Location:INTRON

Gene Symbol:NRP1
Accession:XM_011519755
Location:INTRON

Gene Symbol:NRP1
Accession:XM_006717521
Location:INTRON

Gene Symbol:NRP1
Accession:XM_006717525
Location:INTRON

Gene Symbol:NRP1
Accession:XM_006717524
Location:INTRON

Gene Symbol:NRP1
Accession:NM_001244972
Location:INTRON

Gene Symbol:NRP1
Accession:XM_047425977
Location:INTRON

Gene Symbol:NRP1
Accession:XM_047425978
Location:INTRON

Gene Symbol:NRP1
Accession:XM_006717526
Location:INTRON

Gene Symbol:NRP1
Accession:NR_045259
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000950186 CLINVAR
  RCV003943020 CLINVAR
dbSNP (RS) rs199689769 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NRP1 CLINVAR
OMIM 602069 CLINVAR