RGD:11584368 Rat Genome Database

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Variant: RGD:11584368 -  Homo sapiens

RGD ID: 11584368
RS ID: rs1411578
ClinVar ID: CV303740
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB23  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 57,054,843
GRCh38 6 57,190,045
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012170.1:g.37236G>C
NC_000006.12:g.57190045C>G
NC_000006.11:g.57054843C>G
NM_183227.2:c.*416G>C
More... 		06/14/2016 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RAB23
Accession:NM_001278667
Location:3UTRS;EXON

Gene Symbol:RAB23
Accession:NM_001278666
Location:3UTRS;EXON

Gene Symbol:RAB23
Accession:NM_016277
Location:3UTRS;EXON

Gene Symbol:RAB23
Accession:NM_183227
Location:3UTRS;EXON

Gene Symbol:RAB23
Accession:NM_001278668
Location:3UTRS;EXON

Gene Symbol:RAB23
Accession:NR_103822
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000273177 CLINVAR
dbSNP (RS) rs1411578 CLINVAR
MedGen C1275078 CLINVAR
NCBI Gene RAB23 CLINVAR
OMIM 606144 CLINVAR