RGD:11607964 Rat Genome Database

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Variant: RGD:11607964 -  Homo sapiens

RGD ID: 11607964
RS ID: rs78270485
ClinVar ID: CV310252
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB18  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 27,830,109
GRCh38 10 27,541,180
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_032035.1:g.42007C>T
NC_000010.11:g.27541180C>T
NC_000010.10:g.27830109C>T
NM_001256411.2:c.*3089C>T
More... 		01/12/2018 3 prime utr variant benign|likely benign
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_021252
Location:3UTRS;EXON

Gene Symbol:RAB18
Accession:NM_001256412
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 RCV000349564 CLINVAR
dbSNP (RS) rs78270485 CLINVAR
MedGen C3280203 CLINVAR
NCBI Gene RAB18 CLINVAR
OMIM 602207 CLINVAR
  614222 CLINVAR