RGD:13462797 Rat Genome Database

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Variant: RGD:13462797 -  Homo sapiens

RGD ID: 13462797
RS ID: rs753306232
ClinVar ID: CV439348
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: RLIM  
Reference Nucleotide: AA
Variant Nucleotide: --
Position
Assembly Chr Position
GRCh37 X 73,815,846 - 73,815,848
GRCh38 X 74,596,011 - 74,596,013
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_016120.4:c.-23-12_-23-11del
NM_183353.3:c.-23-12_-23-11del
NG_013258.1:g.23615_23616del
NC_000023.11:g.74596013_74596014del
More... 		02/24/2017 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RLIM
Accession:NM_016120
Location:5UTRS;INTRON

Gene Symbol:RLIM
Accession:NM_183353
Location:5UTRS;INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000514839 CLINVAR
dbSNP (RS) rs753306232 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene RLIM CLINVAR
OMIM 300379 CLINVAR