rs886059164 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: rs886059164 -  Homo sapiens

RGD ID: 11648202
RS ID: rs886059164
ClinVar ID: CV292546
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRAT  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 155,670,617
GRCh38 4 154,749,465
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_009110.1:g.10455T>C
NC_000004.12:g.154749465T>C
NC_000004.11:g.155670617T>C
NM_004744.3:c.*329T>C
More...
01/13/2018 3 prime utr variant uncertain significance Inherited retinal dystrophy; Tapetoretinal degeneration
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:LRAT
Accession:NM_004744
Location:3UTRS;EXON

Gene Symbol:LRAT
Accession:NM_001301645
Location:3UTRS;EXON

Gene Symbol:LRAT
Accession:XM_047416405
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000280529 CLINVAR
  RCV000335676 CLINVAR
  RCV000406747 CLINVAR
dbSNP (RS) rs886059164 CLINVAR
MedGen C0035334 CLINVAR
  C0854723 CLINVAR
  C2750063 CLINVAR
NCBI Gene LRAT CLINVAR
OMIM 268000 CLINVAR
  604863 CLINVAR
  613341 CLINVAR
SNOMED CT 28835009 CLINVAR
  314407005 CLINVAR