rs1234431409 Rat Genome Database

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Variant: rs1234431409 -  Homo sapiens

RGD ID: 152120261
RS ID: rs1234431409
ClinVar ID: CV1593774
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MTOR  MTOR-AS1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 11,206,716
GRCh38 1 11,146,659
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001386501.1:c.3438+17A>G
NM_001386500.1:c.4686+17A>G
NM_004958.4:c.4686+17A>G
LRG_734:g.120893A>G
More... 		09/10/2023 intron variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:MTOR
Accession:XM_047416721
Location:INTRON

Gene Symbol:MTOR
Accession:NM_001386500
Location:INTRON

Gene Symbol:MTOR
Accession:NM_001386501
Location:INTRON

Gene Symbol:MTOR
Accession:XM_047416724
Location:INTRON

Gene Symbol:MTOR
Accession:NM_004958
Location:INTRON

Gene Symbol:MTOR
Accession:XM_017000900
Location:INTRON

Gene Symbol:MTOR
Accession:XM_011541166
Location:INTRON

Gene Symbol:MTOR
Accession:XR_007058581
Location:INTRON;NON-CODING

Gene Symbol:MTOR-AS1
Accession:NR_046600
Location:INTRON;NON-CODING

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002098048 CLINVAR
dbSNP (RS) rs1234431409 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MTOR CLINVAR
  MTOR-AS1 CLINVAR
OMIM 601231 CLINVAR