RGD:11611174 Rat Genome Database

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Variant: RGD:11611174 -  Homo sapiens

RGD ID: 11611174
RS ID: rs11598268
ClinVar ID: CV315389
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB18  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 27,830,464
GRCh38 10 27,541,535
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001256412.2:c.*3484T>C
NG_032035.1:g.42362T>C
NC_000010.11:g.27541535T>C
NC_000010.10:g.27830464T>C
More...
06/14/2016 3 prime utr variant benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RAB18
Accession:NM_021252
Location:3UTRS;EXON

Gene Symbol:RAB18
Accession:NM_001256410
Location:3UTRS;EXON

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000391506 CLINVAR
dbSNP (RS) rs11598268 CLINVAR
MedGen C3280203 CLINVAR
NCBI Gene RAB18 CLINVAR
OMIM 602207 CLINVAR
  614222 CLINVAR