RGD:8652547 Rat Genome Database

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Variant: RGD:8652547 -  Homo sapiens

RGD ID: 8652547
ClinVar ID: CV129122
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HTR3B  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 113,795,492
GRCh38 11 113,924,770
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006028.4:c.214-6614T>C
NG_011483.1:g.24904T>C
NC_000011.10:g.113924770T>C
NC_000011.9:g.113795492T>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:HTR3B
Accession:XM_024448767
Location:5UTRS;INTRON

Gene Symbol:HTR3B
Accession:XM_017018552
Location:INTRON

Gene Symbol:HTR3B
Accession:XM_047427869
Location:INTRON

Gene Symbol:HTR3B
Accession:NM_006028
Location:INTRON

Gene Symbol:HTR3B
Accession:NM_001363563
Location:INTRON

Variant Samples