rs543240181 Rat Genome Database

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Variant: rs543240181 -  Homo sapiens

RGD ID: 11579945
RS ID: rs543240181
ClinVar ID: CV280885
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LEFTY2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 226,124,570
GRCh38 1 225,936,870
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.9351C>G
NC_000001.11:g.225936870G>C
NC_000001.10:g.226124570G>C
NM_003240.3:c.*571C>G
More...
01/13/2018 3 prime utr variant uncertain significance
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 Information

Database Acc Id Source(s)
ClinVar RCV000317507 CLINVAR
dbSNP (RS) rs543240181 CLINVAR
MedGen C1866091 CLINVAR
NCBI Gene LEFTY2 CLINVAR
OMIM 601877 CLINVAR