RGD:28888546 Rat Genome Database

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Variant: RGD:28888546 -  Homo sapiens

RGD ID: 28888546
RS ID: rs192411588
ClinVar ID: CV864238
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SELENON  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 26,142,272
GRCh38 1 25,815,781
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_206926.2:c.*63C>T
NG_009930.1:g.20606C>T
NM_020451.2:c.*63C>T
NM_020451.3:c.*63C>T
More... 		01/13/2018 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SELENON
Accession:NM_020451
Location:3UTRS;EXON

Gene Symbol:SELENON
Accession:NM_206926
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001099132 CLINVAR
dbSNP (RS) rs192411588 CLINVAR
MedGen CN239420 CLINVAR
NCBI Gene SELENON CLINVAR
OMIM 606210 CLINVAR