RGD:150422321 Rat Genome Database

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Variant: RGD:150422321 -  Homo sapiens

RGD ID: 150422321
RS ID: rs12657863
ClinVar ID: CV1193585
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MSX2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 174,155,857
GRCh38 5 174,728,854
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001363626.2:c.*4-305C>T
NM_002449.5:c.380-305C>T
NG_008124.1:g.9283C>T
NC_000005.10:g.174728854C>T
More... 		10/16/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MSX2
Accession:NM_001363626
Location:3UTRS;INTRON

Gene Symbol:MSX2
Accession:NM_002449
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001570988 CLINVAR
dbSNP (RS) rs12657863 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MSX2 CLINVAR
OMIM 123101 CLINVAR