RGD:12837859 Rat Genome Database

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Variant: RGD:12837859 -  Homo sapiens

RGD ID: 12837859
RS ID: rs771669817
ClinVar ID: CV368387
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: STT3B  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 31,656,709
GRCh38 3 31,615,217
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_034164.1:g.87717A>G
NC_000003.12:g.31615217A>G
NC_000003.11:g.31656709A>G
NM_178862.2:c.976+14A>G
More... 		08/18/2016 intron variant likely benign AllHighlyPenetrant

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 RCV000425898 CLINVAR
dbSNP (RS) rs771669817 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene STT3B CLINVAR
OMIM 608605 CLINVAR