rs114492272 Rat Genome Database

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Variant: rs114492272 -  Homo sapiens

RGD ID: 11587102
RS ID: rs114492272
ClinVar ID: CV281008
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LEFTY2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 226,124,824
GRCh38 1 225,937,124
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008118.1:g.9097C>G
NC_000001.11:g.225937124G>C
NC_000001.10:g.226124824G>C
NM_003240.3:c.*317C>G
More...
04/27/2017 3 prime utr variant likely benign none provided
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LEFTY2
Accession:NM_003240
Location:3UTRS;EXON

Gene Symbol:LEFTY2
Accession:NM_001172425
Location:3UTRS;EXON

Gene Symbol:LEFTY2
Accession:XM_011544266
Location:3UTRS;EXON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000292477 CLINVAR
  RCV004710768 CLINVAR
dbSNP (RS) rs114492272 CLINVAR
MedGen C1866091 CLINVAR
  C3661900 CLINVAR
NCBI Gene LEFTY2 CLINVAR
OMIM 601877 CLINVAR