RGD:155267530 Rat Genome Database

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Variant: RGD:155267530 -  Homo sapiens

RGD ID: 155267530
ClinVar ID: CV1704972
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD40  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 44,751,645
GRCh38 20 46,123,006
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.44751645A>T
NM_001322421.2:c.404-120A>T
NC_000020.11:g.46123006A>T
NM_001302753.2:c.404-120A>T
More... 		06/06/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CD40
Accession:XM_017028136
Location:INTRON

Gene Symbol:CD40
Accession:NM_001250
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:CD40
Accession:NM_001322422
Location:INTRON

Gene Symbol:CD40
Accession:NM_152854
Location:INTRON

Gene Symbol:CD40
Accession:NM_001424339
Location:INTRON

Gene Symbol:CD40
Accession:XM_017028135
Location:INTRON

Gene Symbol:CD40
Accession:NM_001302753
Location:INTRON

Gene Symbol:CD40
Accession:XM_011529109
Location:INTRON

Gene Symbol:CD40
Accession:XM_047440601
Location:INTRON

Gene Symbol:CD40
Accession:NM_001322421
Location:INTRON

Gene Symbol:CD40
Accession:NM_001362758
Location:INTRON

Gene Symbol:CD40
Accession:NR_126502
Location:INTRON;NON-CODING

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002285577 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene CD40 CLINVAR
OMIM 109535 CLINVAR