RGD:150516367 Rat Genome Database

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Variant: RGD:150516367 -  Homo sapiens

RGD ID: 150516367
RS ID: rs7258655
ClinVar ID: CV1228322
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GNA11  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 3,113,770
GRCh38 19 3,113,772
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1111:g.24363T>C
NG_033852.2:g.24363T>C
NC_000019.10:g.3113772T>C
NC_000019.9:g.3113770T>C
More... 		11/12/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GNA11
Accession:NM_002067
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001639128 CLINVAR
dbSNP (RS) rs7258655 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GNA11 CLINVAR
OMIM 139313 CLINVAR