RGD:8582086 Rat Genome Database

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Variant: RGD:8582086 -  Homo sapiens

RGD ID: 8582086
ClinVar ID: CV116554
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EYS  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 66,339,745
GRCh38 6 65,629,852
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.-333+9926T>G
NG_023443.1:g.82374T>G
NC_000006.12:g.65629852A>C
NC_000006.11:g.66339745A>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:EYS
Accession:NM_001292009
Location:5UTRS;INTRON

Gene Symbol:EYS
Accession:NM_001142800
Location:5UTRS;INTRON

Gene Symbol:EYS
Accession:NM_001142801
Location:5UTRS;INTRON

Gene Symbol:EYS
Accession:NM_198283
Location:INTRON

Variant Samples