RGD:11598809 Rat Genome Database

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Variant: RGD:11598809 -  Homo sapiens

RGD ID: 11598809
RS ID: rs767741672
ClinVar ID: CV322045
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB18  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 27,829,842
GRCh38 10 27,540,913
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021252.5:c.*2862T>C
NM_021252.4:c.*2862T>C
NM_001256411.2:c.*2822T>C
NM_001256412.2:c.*2862T>C
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RAB18
Accession:NM_001256410
Location:3UTRS;EXON

Gene Symbol:RAB18
Accession:NM_001256412
Location:3UTRS;EXON

Gene Symbol:RAB18
Accession:NM_021252
Location:3UTRS;EXON

Gene Symbol:RAB18
Accession:NM_001256411
Location:3UTRS;EXON

Gene Symbol:RAB18
Accession:NR_046172
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000260500 CLINVAR
dbSNP (RS) rs767741672 CLINVAR
MedGen C3280203 CLINVAR
NCBI Gene RAB18 CLINVAR
OMIM 602207 CLINVAR
  614222 CLINVAR