RGD:152170570 Rat Genome Database

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Variant: RGD:152170570 -  Homo sapiens

RGD ID: 152170570
RS ID: rs761736586
ClinVar ID: CV1592489
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATP2A2  LOC126861638  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 110,783,197
GRCh38 12 110,345,392
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001681.4:c.2741+10C>T
NM_170665.4:c.2741+10C>T
NG_007097.2:g.68766C>T
NC_000012.12:g.110345392C>T
More... 		10/15/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ATP2A2
Accession:NM_170665
Location:INTRON

Gene Symbol:ATP2A2
Accession:NM_001681
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ATP2A2
Accession:XM_011538402
Location:INTRON

Gene Symbol:ATP2A2
Accession:NM_001413015
Location:INTRON

Gene Symbol:ATP2A2
Accession:NM_001413014
Location:INTRON

Gene Symbol:ATP2A2
Accession:NM_001413013
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002161817 CLINVAR
dbSNP (RS) rs761736586 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ATP2A2 CLINVAR
  LOC126861638 CLINVAR
OMIM 108740 CLINVAR