rs3814658 Rat Genome Database

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Variant: rs3814658 -  Homo sapiens

RGD ID: 150411648
RS ID: rs3814658
ClinVar ID: CV1177269
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OPTN  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 13,160,654
GRCh38 10 13,118,654
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NC_000010.11:g.13118654T>C
NC_000010.10:g.13160654T>C
NM_001008211.1:c.627-234T>C
NM_001008212.2:c.627-234T>C
More... 		08/31/2018 intron variant likely benign none provided

Gene Symbol:OPTN
Accession:NM_001008212
Location:INTRON

Gene Symbol:OPTN
Accession:NM_001008213
Location:INTRON

Gene Symbol:OPTN
Accession:NM_001008211
Location:INTRON

Gene Symbol:OPTN
Accession:NM_021980
Location:INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001547247 CLINVAR
dbSNP (RS) rs3814658 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene OPTN CLINVAR
OMIM 602432 CLINVAR