RGD:8587690 Rat Genome Database

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Variant: RGD:8587690 -  Homo sapiens

RGD ID: 8587690
ClinVar ID: CV122321
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RPS6KA6  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 83,329,871
GRCh38 X 84,074,863
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_014496.4:c.1972-9752T>C
NG_016340.1:g.118073T>C
NC_000023.11:g.84074863A>G
NC_000023.10:g.83329871A>G
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:RPS6KA6
Accession:XM_011530919
Location:INTRON

Gene Symbol:RPS6KA6
Accession:XM_017029425
Location:INTRON

Gene Symbol:RPS6KA6
Accession:XM_017029424
Location:INTRON

Gene Symbol:RPS6KA6
Accession:XM_011530920
Location:INTRON

Gene Symbol:RPS6KA6
Accession:XM_017029423
Location:INTRON

Gene Symbol:RPS6KA6
Accession:NM_001330512
Location:INTRON

Gene Symbol:RPS6KA6
Accession:XM_011530917
Location:INTRON

Gene Symbol:RPS6KA6
Accession:XM_047441997
Location:INTRON

Gene Symbol:RPS6KA6
Accession:XM_047441996
Location:INTRON

Gene Symbol:RPS6KA6
Accession:NM_014496
Location:INTRON

Variant Samples