RGD:156041278 Rat Genome Database

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Variant: RGD:156041278 -  Homo sapiens

RGD ID: 156041278
ClinVar ID: CV1891057
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARID1A  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 27,099,994
GRCh38 1 26,773,503
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_006015.6:c.3866+7A>T
NM_139135.4:c.3866+7A>T
LRG_875:g.82473A>T
NG_029965.1:g.82473A>T
More... 		07/14/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ARID1A
Accession:NM_139135
Location:INTRON

Gene Symbol:ARID1A
Accession:NM_006015
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003078527 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ARID1A CLINVAR
OMIM 603024 CLINVAR