RGD:15151491 Rat Genome Database

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Variant: RGD:15151491 -  Homo sapiens

RGD ID: 15151491
RS ID: rs117840373
ClinVar ID: CV730632
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RPS6  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 19,378,520
GRCh38 9 19,378,522
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001010.3:c.350-8C>G
NC_000009.12:g.19378522G>C
NC_000009.11:g.19378520G>C
NM_001010.2:c.350-8C>G
 01/16/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RPS6
Accession:NM_001010
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000879606 CLINVAR
dbSNP (RS) rs117840373 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RPS6 CLINVAR
OMIM 180460 CLINVAR