RGD:156395701 Rat Genome Database

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Variant: RGD:156395701 -  Homo sapiens

RGD ID: 156395701
ClinVar ID: CV1928029
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126862065  TRAF3  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 14 103,352,619
GRCh38 14 102,886,282
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001199427.2:c.570+9757G>C
NM_001385143.1:c.571-3278G>C
NM_001385142.1:c.651+13G>C
NM_003300.4:c.651+13G>C
More... 		04/16/2022 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:TRAF3
Accession:NM_145725
Location:INTRON

Gene Symbol:TRAF3
Accession:NM_145726
Location:INTRON

Gene Symbol:TRAF3
Accession:NM_003300
Location:INTRON

Gene Symbol:TRAF3
Accession:NM_001199427
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_011537118
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_011537117
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_011537116
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_017021620
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_017021617
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_017021619
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_017021618
Location:INTRON

Gene Symbol:TRAF3
Accession:NM_001385142
Location:INTRON

Gene Symbol:TRAF3
Accession:NM_001385143
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_047431739
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_047431742
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_047431740
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_047431738
Location:INTRON

Gene Symbol:TRAF3
Accession:XM_047431741
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002654888 CLINVAR
MedGen C3553868 CLINVAR
NCBI Gene LOC126862065 CLINVAR
  TRAF3 CLINVAR
OMIM 601896 CLINVAR
  614849 CLINVAR