RGD:8590911 Rat Genome Database

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Variant: RGD:8590911 -  Homo sapiens

RGD ID: 8590911
ClinVar ID: CV125620
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LINC01446  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 53,863,028
GRCh38 7 53,795,335
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.14:g.53795335C>A
NC_000007.13:g.53863028C>A
NR_038371.1:n.425-15297G>T
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:LINC01446
Accession:NR_038371
Location:INTRON;NON-CODING

Variant Samples