RGD:150539393 Rat Genome Database

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Variant: RGD:150539393 -  Homo sapiens

RGD ID: 150539393
RS ID: rs186926288
ClinVar ID: CV1308747
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: STT3B  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 31,661,421
GRCh38 3 31,619,929
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_178862.3:c.1327+99A>G
NG_034164.1:g.92429A>G
NC_000003.12:g.31619929A>G
NC_000003.11:g.31661421A>G
 05/29/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:STT3B
Accession:XM_017005858
Location:INTRON

Gene Symbol:STT3B
Accession:XM_011533465
Location:INTRON

Gene Symbol:STT3B
Accession:NM_178862
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001766251 CLINVAR
dbSNP (RS) rs186926288 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene STT3B CLINVAR
OMIM 608605 CLINVAR