RGD:150483230 Rat Genome Database

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Variant: RGD:150483230 -  Homo sapiens

RGD ID: 150483230
RS ID: rs60882748
ClinVar ID: CV1261750
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RAB23  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 57,072,804
GRCh38 6 57,208,006
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001278666.2:c.156-293A>G
NM_001278667.2:c.156-293A>G
NM_001278668.2:c.156-293A>G
NM_016277.5:c.156-293A>G
More...
03/24/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RAB23
Accession:NM_016277
Location:INTRON

Gene Symbol:RAB23
Accession:NM_183227
Location:INTRON

Gene Symbol:RAB23
Accession:NM_001278666
Location:INTRON

Gene Symbol:RAB23
Accession:NM_001278667
Location:INTRON

Gene Symbol:RAB23
Accession:NM_001278668
Location:INTRON

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001686354 CLINVAR
dbSNP (RS) rs60882748 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RAB23 CLINVAR
OMIM 606144 CLINVAR