RGD:151885028 Rat Genome Database

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Variant: RGD:151885028 -  Homo sapiens

RGD ID: 151885028
RS ID: rs778995508
ClinVar ID: CV1429040
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD40  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 20 44,756,771
GRCh38 20 46,128,132
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000020.10:g.44756771C>G
NR_126502.2:n.587C>G
NM_001322422.2:c.404-6C>G
NM_152854.4:c.498-6C>G
More...
08/13/2021 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:CD40
Accession:NR_126502
Location:EXON;NON-CODING

Gene Symbol:CD40
Accession:NM_001250
Location:INTRON

Gene Symbol:CD40
Accession:NM_152854
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:CD40
Accession:NM_001302753
Location:INTRON

Gene Symbol:CD40
Accession:XM_011529109
Location:INTRON

Gene Symbol:CD40
Accession:NM_001322421
Location:INTRON

Gene Symbol:CD40
Accession:NM_001322422
Location:INTRON

Gene Symbol:CD40
Accession:XM_017028135
Location:INTRON

Gene Symbol:CD40
Accession:XM_017028136
Location:INTRON

Gene Symbol:CD40
Accession:NM_001362758
Location:INTRON

Gene Symbol:CD40
Accession:XM_047440601
Location:INTRON

Gene Symbol:CD40
Accession:NR_136327
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002000396 CLINVAR
dbSNP (RS) rs778995508 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CD40 CLINVAR
OMIM 109535 CLINVAR