RGD:150437240 Rat Genome Database

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Variant: RGD:150437240 -  Homo sapiens

RGD ID: 150437240
RS ID: rs539222462
ClinVar ID: CV1286513
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: JAM3  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 134,018,891
GRCh38 11 134,148,996
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000011.10:g.134148996T>A
NC_000011.9:g.134018891T>A
NG_028348.1:g.85072T>A
NM_001205329.2:c.745-150T>A
More... 		06/06/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:JAM3
Accession:NM_032801
Location:INTRON

Gene Symbol:JAM3
Accession:NM_001205329
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001724592 CLINVAR
dbSNP (RS) rs539222462 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene JAM3 CLINVAR
OMIM 606871 CLINVAR