RGD:8577949 Rat Genome Database

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Variant: RGD:8577949 -  Homo sapiens

RGD ID: 8577949
ClinVar ID: CV112326
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FSTL1  LOC124900546  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 120,161,621
GRCh38 3 120,442,774
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000003.12:g.120442774T>A
NC_000003.11:g.120161621T>A
NM_007085.4:c.63+7910A>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:LOC124900546
Accession:XR_007096030
Location:EXON;NON-CODING

Gene Symbol:FSTL1
Accession:NM_007085
Location:INTRON

Variant Samples