rs147661029 Rat Genome Database

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Variant: rs147661029 -  Homo sapiens

RGD ID: 150414336
RS ID: rs147661029
ClinVar ID: CV1177266
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC108903148  OPTN  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 13,150,781
GRCh38 10 13,108,781
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001008212.2:c.-11-331C>T
NM_021980.4:c.-11-331C>T
NM_001008213.1:c.-65-181C>T
NC_000010.10:g.13150781C>T
More... 		05/29/2019 intron variant likely benign none provided

Gene Symbol:OPTN
Accession:NM_021980
Location:5UTRS;INTRON

Gene Symbol:OPTN
Accession:NM_001008213
Location:5UTRS;INTRON

Gene Symbol:OPTN
Accession:NM_001008212
Location:5UTRS;INTRON

Gene Symbol:OPTN
Accession:NM_001008211
Location:5UTRS;INTRON

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Database
Acc Id
Source(s)
ClinVar RCV001548082 CLINVAR
dbSNP (RS) rs147661029 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC108903148 CLINVAR
  OPTN CLINVAR
OMIM 602432 CLINVAR