RGD:8586658 Rat Genome Database

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Variant: RGD:8586658 -  Homo sapiens

RGD ID: 8586658
ClinVar ID: CV121262
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PAK5  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 20 9,623,649
GRCh38 20 9,643,001
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000020.11:g.9643001T>C
NC_000020.10:g.9623649T>C
NM_020341.3:c.204+1124A>G
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:PAK5
Accession:NM_177990
Location:INTRON

Gene Symbol:PAK5
Accession:XM_017027965
Location:INTRON

Gene Symbol:PAK5
Accession:XM_017027961
Location:INTRON

Gene Symbol:PAK5
Accession:NM_020341
Location:INTRON

Gene Symbol:PAK5
Accession:XM_017027964
Location:INTRON

Gene Symbol:PAK5
Accession:XM_017027960
Location:INTRON

Gene Symbol:PAK5
Accession:XM_017027962
Location:INTRON

Variant Samples