RGD:8579912 Rat Genome Database

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Variant: RGD:8579912 -  Homo sapiens

RGD ID: 8579912
ClinVar ID: CV114314
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124900165  STX18-AS1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 4,646,023
GRCh38 4 4,644,296
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000004.12:g.4644296G>C
NC_000004.11:g.4646023G>C
NR_037888.1:n.516-4681G>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:LOC124900165
Accession:XM_047416488
Location:5UTRS;INTRON

Gene Symbol:LOC124900165
Accession:XM_047416487
Location:5UTRS;INTRON

Gene Symbol:LOC124900165
Accession:XM_047416492
Location:5UTRS;INTRON

Gene Symbol:LOC124900165
Accession:XM_047416489
Location:5UTRS;INTRON

Gene Symbol:LOC124900165
Accession:XM_047416486
Location:5UTRS;INTRON

Gene Symbol:LOC124900165
Accession:XM_047416485
Location:5UTRS;INTRON

Gene Symbol:LOC124900165
Accession:XM_047416491
Location:5UTRS;INTRON

Gene Symbol:LOC124900165
Accession:XM_047416490
Location:5UTRS;INTRON

Gene Symbol:STX18-AS1
Accession:NR_037888
Location:INTRON;NON-CODING

Variant Samples