RGD:8575963 Rat Genome Database

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Variant: RGD:8575963 -  Homo sapiens

RGD ID: 8575963
ClinVar ID: CV110318
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TRABD2B  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 48,244,514
GRCh38 1 47,778,842
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.47778842A>G
NC_000001.10:g.48244514A>G
NM_001194986.1:c.989-298T>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:TRABD2B
Accession:NM_001194986
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_006710640
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_011541443
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_011541445
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_011541444
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_017001262
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_017001263
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_017001261
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_017001260
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_024446933
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_024446935
Location:INTRON

Gene Symbol:TRABD2B
Accession:XM_047420060
Location:INTRON

Variant Samples