RGD:150481331 Rat Genome Database

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Variant: RGD:150481331 -  Homo sapiens

RGD ID: 150481331
RS ID: rs33946149
ClinVar ID: CV1238484
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MSX1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 4,864,301
GRCh38 4 4,862,574
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1342t1:c.470-127C>A
NM_002448.3:c.470-127C>A
LRG_1342:g.7910C>A
NG_008121.1:g.7910C>A
More... 		05/14/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MSX1
Accession:NM_002448
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001652925 CLINVAR
dbSNP (RS) rs33946149 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MSX1 CLINVAR
OMIM 142983 CLINVAR