RGD:8583168 Rat Genome Database

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Variant: RGD:8583168 -  Homo sapiens

RGD ID: 8583168
ClinVar ID: CV117728
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TBC1D4  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 13 76,021,379
GRCh38 13 75,447,243
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000013.11:g.75447243T>C
NC_000013.10:g.76021379T>C
NM_001286658.1:c.498+34027A>G
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:TBC1D4
Accession:NM_001286658
Location:INTRON

Gene Symbol:TBC1D4
Accession:NM_001286659
Location:INTRON

Gene Symbol:TBC1D4
Accession:XM_047430812
Location:INTRON

Gene Symbol:TBC1D4
Accession:XM_005266603
Location:INTRON

Gene Symbol:TBC1D4
Accession:XM_047430811
Location:INTRON

Gene Symbol:TBC1D4
Accession:XM_047430809
Location:INTRON

Gene Symbol:TBC1D4
Accession:XM_006719903
Location:INTRON

Gene Symbol:TBC1D4
Accession:XM_011535331
Location:INTRON

Gene Symbol:TBC1D4
Accession:NM_014832
Location:INTRON

Gene Symbol:TBC1D4
Accession:XM_047430808
Location:INTRON

Gene Symbol:TBC1D4
Accession:XM_047430810
Location:INTRON

Variant Samples