RGD:11610653 Rat Genome Database

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Variant: RGD:11610653 -  Homo sapiens

RGD ID: 11610653
RS ID: rs41318039
ClinVar ID: CV305275
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SIM1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 6 100,838,124
GRCh38 6 100,390,248
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008230.1:g.78428A>T
NC_000006.12:g.100390248T>A
NC_000006.11:g.100838124T>A
NM_001374769.1:c.*113A>T
More... 		01/12/2018 3 prime utr variant benign|likely benign
Disease Annotations     Click to see Annotation Detail View
obesity  (IAGP)


Variant Details
Variant Transcripts
Gene Symbol:SIM1
Accession:NM_001374769
Location:3UTRS;EXON

Gene Symbol:SIM1
Accession:NM_005068
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000384192 CLINVAR
dbSNP (RS) rs41318039 CLINVAR
MedGen C5191050 CLINVAR
NCBI Gene SIM1 CLINVAR
OMIM 603128 CLINVAR