RGD:150543402 Rat Genome Database

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Variant: RGD:150543402 -  Homo sapiens

RGD ID: 150543402
RS ID: rs138224601
ClinVar ID: CV1309442
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GNAO1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 56,380,338
GRCh38 16 56,346,426
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_138736.3:c.*2476G>A
NM_020988.3:c.724-4958G>A
NG_042800.1:g.160088G>A
NC_000016.10:g.56346426G>A
More... 		11/03/2021 3 prime utr variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:GNAO1
Accession:NM_138736
Location:3UTRS;EXON

Gene Symbol:GNAO1
Accession:XR_007064866
Location:EXON;NON-CODING

Gene Symbol:GNAO1
Accession:NM_020988
Location:INTRON

Gene Symbol:GNAO1
Accession:XM_011523003
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003238509 CLINVAR
dbSNP (RS) rs138224601 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GNAO1 CLINVAR
OMIM 139311 CLINVAR