RGD:28884159 Rat Genome Database

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Variant: RGD:28884159 -  Homo sapiens

RGD ID: 28884159
RS ID: rs1241475769
ClinVar ID: CV890288
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRAT  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 155,670,426
GRCh38 4 154,749,274
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004744.5:c.*138C>A
NG_009110.1:g.10264C>A
NM_004744.3:c.*138C>A
NC_000004.12:g.154749274C>A
More... 		04/27/2017 3 prime utr variant uncertain significance 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 RCV001144385 CLINVAR
  RCV001150479 CLINVAR
dbSNP (RS) rs1241475769 CLINVAR
MedGen C0035334 CLINVAR
  C2750063 CLINVAR
NCBI Gene LRAT CLINVAR
OMIM 268000 CLINVAR
  604863 CLINVAR
  613341 CLINVAR
SNOMED CT 28835009 CLINVAR