RGD:8582077 Rat Genome Database

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Variant: RGD:8582077 -  Homo sapiens

RGD ID: 8582077
ClinVar ID: CV116545
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EYS  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 66,024,821
GRCh38 6 65,314,928
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001142800.1:c.1767-18809T>A
NG_023443.1:g.397298T>A
NC_000006.12:g.65314928A>T
NC_000006.11:g.66024821A>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:EYS
Accession:NM_001142800
Location:INTRON

Gene Symbol:EYS
Accession:NM_001292009
Location:INTRON

Gene Symbol:EYS
Accession:NM_001142801
Location:INTRON

Gene Symbol:EYS
Accession:NM_198283
Location:INTRON

Variant Samples