RGD:12836864 Rat Genome Database

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Variant: RGD:12836864 -  Homo sapiens

RGD ID: 12836864
RS ID: rs185338981
ClinVar ID: CV371296
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: STT3A  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 125,475,509
GRCh38 11 125,605,614
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001278503.2:c.509-15G>T
NM_152713.5:c.509-15G>T
NG_042806.1:g.17820G>T
NC_000011.10:g.125605614G>T
More... 		11/01/2021 intron variant benign|likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:STT3A
Accession:NM_001278503
Location:INTRON

Gene Symbol:STT3A
Accession:XM_047426898
Location:INTRON

Gene Symbol:STT3A
Accession:NM_001278504
Location:INTRON

Gene Symbol:STT3A
Accession:NM_152713
Location:INTRON

Gene Symbol:STT3A
Accession:XM_011542807
Location:INTRON

Gene Symbol:STT3A
Accession:XM_047426897
Location:INTRON

Gene Symbol:STT3A
Accession:XM_047426895
Location:INTRON

Gene Symbol:STT3A
Accession:XM_047426896
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001720196 CLINVAR
dbSNP (RS) rs185338981 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene STT3A CLINVAR
OMIM 601134 CLINVAR