RGD:15124350 Rat Genome Database

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Variant: RGD:15124350 -  Homo sapiens

RGD ID: 15124350
RS ID: rs10083677
ClinVar ID: CV744785
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD276  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 73,995,993
GRCh38 15 73,703,652
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_025240.3:c.419-524C>T
NM_001329629.2:c.296-7C>T
NM_001329628.2:c.419-524C>T
NM_001024736.2:c.734-7C>T
More... 		12/04/2017 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CD276
Accession:XM_011522095
Location:INTRON

Gene Symbol:CD276
Accession:NM_001024736
Location:INTRON

Gene Symbol:CD276
Accession:NM_001329628
Location:INTRON

Gene Symbol:CD276
Accession:XM_005254700
Location:INTRON

Gene Symbol:CD276
Accession:NM_025240
Location:INTRON

Gene Symbol:CD276
Accession:NM_001329629
Location:INTRON

Gene Symbol:CD276
Accession:XM_047433147
Location:INTRON

Gene Symbol:CD276
Accession:XM_017022638
Location:INTRON

Gene Symbol:CD276
Accession:XM_047433148
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000896573 CLINVAR
dbSNP (RS) rs10083677 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CD276 CLINVAR
OMIM 605715 CLINVAR