RGD:14707056 Rat Genome Database

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Variant: RGD:14707056 -  Homo sapiens

RGD ID: 14707056
RS ID: rs9435269
ClinVar ID: CV658030
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PLEKHG5  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 6,527,745
GRCh38 1 6,467,685
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007978.1:g.57325G>A
NC_000001.11:g.6467685C>T
NC_000001.10:g.6527745C>T
NM_020631.4:c.3012-113G>A
More... 		06/18/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:PLEKHG5
Accession:NM_001265594
Location:3UTRS;INTRON

Gene Symbol:PLEKHG5
Accession:NM_198681
Location:INTRON

Gene Symbol:PLEKHG5
Accession:NM_001042663
Location:INTRON

Gene Symbol:PLEKHG5
Accession:NM_001042665
Location:INTRON

Gene Symbol:PLEKHG5
Accession:NM_020631
Location:INTRON

Gene Symbol:PLEKHG5
Accession:NM_001265593
Location:INTRON

Gene Symbol:PLEKHG5
Accession:NM_001265592
Location:INTRON

Gene Symbol:PLEKHG5
Accession:NM_001042664
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000826715 CLINVAR
dbSNP (RS) rs9435269 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PLEKHG5 CLINVAR
OMIM 611101 CLINVAR