rs2736911 Rat Genome Database

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Variant: rs2736911 -  Homo sapiens

RGD ID: 11605186
RS ID: rs2736911
ClinVar ID: CV314432
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARMS2  LOC105378525  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 124,214,355
GRCh38 10 122,454,839
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001099667.1:c.112C>T
NG_011725.1:g.5177C>T
NC_000010.11:g.122454839C>T
NC_000010.10:g.124214355C>T
More... 		03/06/2018 nonsense benign|likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ARMS2
Accession:NM_001099667
Location:EXON
Amino Acid Prediction: R to * (nonsynonymous)
Amino Acid Position: 38
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MLRLYPGPMVTEAEGKGGPEMASLSSSVVPVSFISTL*ESVLDPGVGGEGASDKQRSKLSLSHSMIPAAKIHTELCLPAF
FSPAGTQRRFQQPQHHLTLSIIHTAAR*

Gene Symbol:LOC105378525
Accession:XR_946384
Location:INTRON;NON-CODING

Gene Symbol:LOC105378525
Accession:XR_946383
Location:INTRON;NON-CODING

Gene Symbol:LOC105378525
Accession:XR_946385
Location:INTRON;NON-CODING

Gene Symbol:LOC105378525
Accession:XR_946382
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000316955 CLINVAR
  RCV003983000 CLINVAR
dbSNP (RS) rs2736911 CLINVAR
GWAS Catalog GCST90104786 GWAS Catalog
MedGen C3151070 CLINVAR
NCBI Gene ARMS2 CLINVAR
OMIM 611313 CLINVAR
  613778 CLINVAR