RGD:156416778 Rat Genome Database

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Variant: RGD:156416778 -  Homo sapiens

RGD ID: 156416778
ClinVar ID: CV1969999
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: JAM3  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 134,014,908
GRCh38 11 134,145,013
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001205329.2:c.459+19G>C
NM_032801.5:c.612+19G>C
NG_028348.1:g.81089G>C
NC_000011.10:g.134145013G>C
More... 		10/08/2022 intron variant uncertain significance 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 References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002589871 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene JAM3 CLINVAR
OMIM 606871 CLINVAR