RGD:13592675 Rat Genome Database

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Variant: RGD:13592675 -  Homo sapiens

RGD ID: 13592675
RS ID: rs903798730
ClinVar ID: CV498594
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SELENON  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 26,140,681
GRCh38 1 25,814,190
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.10:g.26140681C>T
NG_009930.1:g.19015C>T
NC_000001.11:g.25814190C>T
NM_020451.3:c.1602+12C>T
More... 		03/17/2017 intron variant likely benign AllHighlyPenetrant

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 RCV000606957 CLINVAR
dbSNP (RS) rs903798730 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene SELENON CLINVAR
OMIM 606210 CLINVAR