RGD:150406749 Rat Genome Database

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Variant: RGD:150406749 -  Homo sapiens

RGD ID: 150406749
RS ID: rs139633798
ClinVar ID: CV1195074
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GNAO1-DT  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 56,224,940
GRCh38 16 56,191,028
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000016.10:g.56191028G>A
NC_000016.9:g.56224940G>A
NG_042800.1:g.4690G>A
NR_027078.2:n.67C>T
 09/29/2018 non-coding transcript variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GNAO1-DT
Accession:NR_027078
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001572116 CLINVAR
dbSNP (RS) rs139633798 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GNAO1 CLINVAR
  GNAO1-DT CLINVAR
OMIM 139311 CLINVAR