RGD:8583410 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: RGD:8583410 -  Homo sapiens

RGD ID: 8583410
ClinVar ID: CV117971
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HS6ST3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 13 97,047,154
GRCh38 13 96,394,900
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000013.11:g.96394900G>A
NC_000013.10:g.97047154G>A
NM_153456.3:c.707+303331G>A
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:HS6ST3
Accession:NM_153456
Location:INTRON

Variant Samples