RGD:405197752 Rat Genome Database

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Variant: RGD:405197752 -  Homo sapiens

RGD ID: 405197752
ClinVar ID: CV3168305
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATP1A1  ATP1A1-AS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 116,946,490
GRCh38 1 116,403,868
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001160234.2:c.2859-16C>T
NM_000701.8:c.2952-16C>T
NM_001160233.2:c.2952-16C>T
NG_047036.1:g.36684C>T
More... 		10/25/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ATP1A1
Accession:NM_000701
Location:INTRON

Gene Symbol:ATP1A1
Accession:NM_001160233
Location:INTRON

Gene Symbol:ATP1A1
Accession:NM_001160234
Location:INTRON

Gene Symbol:ATP1A1-AS1
Accession:NR_024125
Location:INTRON;NON-CODING

Gene Symbol:ATP1A1-AS1
Accession:NR_024124
Location:INTRON;NON-CODING

Gene Symbol:ATP1A1-AS1
Accession:NR_024126
Location:INTRON;NON-CODING

Gene Symbol:ATP1A1-AS1
Accession:NR_027646
Location:INTRON;NON-CODING

Gene Symbol:ATP1A1-AS1
Accession:NR_027645
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003860437 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ATP1A1 CLINVAR
  ATP1A1-AS1 CLINVAR
OMIM 182310 CLINVAR
  618305 CLINVAR