RGD:8586120 Rat Genome Database

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Variant: RGD:8586120 -  Homo sapiens

RGD ID: 8586120
ClinVar ID: CV120715
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHST8  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 34,246,978
GRCh38 19 33,756,073
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001127895.1:c.131-15340G>A
NG_029857.1:g.139118G>A
NC_000019.10:g.33756073G>A
NC_000019.9:g.34246978G>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CHST8
Accession:NM_022467
Location:INTRON

Gene Symbol:CHST8
Accession:XM_017027143
Location:INTRON

Gene Symbol:CHST8
Accession:XM_011527222
Location:INTRON

Gene Symbol:CHST8
Accession:NM_001127896
Location:INTRON

Gene Symbol:CHST8
Accession:NM_001127895
Location:INTRON

Gene Symbol:CHST8
Accession:XM_011527224
Location:INTRON

Variant Samples