RGD:8579867 Rat Genome Database

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Variant: RGD:8579867 -  Homo sapiens

RGD ID: 8579867
ClinVar ID: CV114269
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: STX18  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 4 4,496,962
GRCh38 4 4,495,235
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.4495235C>T
NC_000004.11:g.4496962C>T
NM_016930.2:c.169-23529G>A
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:STX18
Accession:NM_001346282
Location:5UTRS;INTRON

Gene Symbol:STX18
Accession:NM_016930
Location:INTRON

Gene Symbol:STX18
Accession:NM_001346281
Location:INTRON

Gene Symbol:STX18
Accession:NM_001346300
Location:INTRON

Gene Symbol:STX18
Accession:NR_144414
Location:INTRON;NON-CODING

Variant Samples