RGD:8586948 Rat Genome Database

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Variant: RGD:8586948 -  Homo sapiens

RGD ID: 8586948
ClinVar ID: CV121571
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TBC1D22A  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 47,234,465
GRCh38 22 46,838,568
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000022.11:g.46838568A>G
NC_000022.10:g.47234465A>G
NM_001284303.1:c.404-40085A>G
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:TBC1D22A
Accession:XM_047441307
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_017028742
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_017028743
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_017028746
Location:INTRON

Gene Symbol:TBC1D22A
Accession:NM_001284303
Location:INTRON

Gene Symbol:TBC1D22A
Accession:NM_001284305
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_011530102
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_047441309
Location:INTRON

Gene Symbol:TBC1D22A
Accession:NM_001284304
Location:INTRON

Gene Symbol:TBC1D22A
Accession:NM_014346
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_047441308
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_047441306
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_017028747
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_011530100
Location:INTRON

Gene Symbol:TBC1D22A
Accession:XM_011530101
Location:INTRON

Gene Symbol:TBC1D22A
Accession:NM_001410803
Location:INTRON

Gene Symbol:TBC1D22A
Accession:NR_104292
Location:INTRON;NON-CODING

Gene Symbol:TBC1D22A
Accession:XR_007067971
Location:INTRON;NON-CODING

Gene Symbol:TBC1D22A
Accession:XR_007067970
Location:INTRON;NON-CODING

Variant Samples