RGD:155945563 Rat Genome Database

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Variant: RGD:155945563 -  Homo sapiens

RGD ID: 155945563
ClinVar ID: CV1911273
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARL13B  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 93,772,013
GRCh38 3 94,053,169
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001321328.2:c.1166-18T>C
NM_001174150.2:c.1211-18T>C
NM_182896.3:c.1211-18T>C
NM_144996.4:c.890-18T>C
More... 		09/20/2022 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ARL13B
Accession:NM_001174150
Location:INTRON

Gene Symbol:ARL13B
Accession:XM_011512535
Location:INTRON

Gene Symbol:ARL13B
Accession:XM_011512533
Location:INTRON

Gene Symbol:ARL13B
Accession:NM_001321328
Location:INTRON

Gene Symbol:ARL13B
Accession:XM_047447661
Location:INTRON

Gene Symbol:ARL13B
Accession:NM_001174151
Location:INTRON

Gene Symbol:ARL13B
Accession:NM_144996
Location:INTRON

Gene Symbol:ARL13B
Accession:XM_006713532
Location:INTRON

Gene Symbol:ARL13B
Accession:XM_011512532
Location:INTRON

Gene Symbol:ARL13B
Accession:XM_017005853
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ARL13B
Accession:NM_001410782
Location:INTRON

Gene Symbol:ARL13B
Accession:NM_182896
Location:INTRON

Gene Symbol:ARL13B
Accession:NR_135621
Location:INTRON;NON-CODING

Gene Symbol:ARL13B
Accession:NR_033427
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002615911 CLINVAR
MedGen C2676771 CLINVAR
NCBI Gene ARL13B CLINVAR
OMIM 608922 CLINVAR
  612291 CLINVAR