RGD:8651644 Rat Genome Database

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Variant: RGD:8651644 -  Homo sapiens

RGD ID: 8651644
ClinVar ID: CV128219
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GFRA1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 117,902,987
GRCh38 10 116,143,476
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000010.11:g.116143476C>G
NC_000010.10:g.117902987C>G
NM_001145453.1:c.419-17919G>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:GFRA1
Accession:NM_001382557
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_001382558
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_001348099
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_001348098
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_001382560
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_001382556
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_005264
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_001382559
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_001348096
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_001382561
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_001145453
Location:INTRON

Gene Symbol:GFRA1
Accession:NM_145793
Location:INTRON

Variant Samples