RGD:14740975 Rat Genome Database

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Variant: RGD:14740975 -  Homo sapiens

RGD ID: 14740975
RS ID: rs6676342
ClinVar ID: CV657739
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SELENON  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 26,127,202
GRCh38 1 25,800,711
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_020451.3:c.183+298T>G
NM_206926.2:c.183+298T>G
NG_009930.1:g.5536T>G
NC_000001.11:g.25800711T>G
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SELENON
Accession:NM_020451
Location:INTRON

Gene Symbol:SELENON
Accession:NM_206926
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000840572 CLINVAR
dbSNP (RS) rs6676342 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SELENON CLINVAR
OMIM 606210 CLINVAR