RGD:407457328 Rat Genome Database

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Variant: RGD:407457328 -  Homo sapiens

RGD ID: 407457328
ClinVar ID: CV3416107
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: B4GALNT1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 58,025,823
GRCh38 12 57,632,040
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001413981.1:c.-811C>T
NM_001413982.1:c.-811C>T
NM_001413983.1:c.-811C>T
NM_001413984.1:c.-811C>T
More... 		07/01/2024 5 prime utr variant likely benign none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

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Database
Acc Id
Source(s)
ClinVar RCV004598985 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene B4GALNT1 CLINVAR
OMIM 601873 CLINVAR