RGD:156355694 Rat Genome Database

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Variant: RGD:156355694 -  Homo sapiens

RGD ID: 156355694
ClinVar ID: CV2165856
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: SMAD2  
Reference Nucleotide: G
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 18 45,368,227
GRCh38 18 47,841,856
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001135937.3:c.1286del
NM_001003652.4:c.1376del
NM_005901.6:c.1376del
NG_029946.2:g.94017del
More... 		07/01/2022 frameshift variant uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV003031215 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SMAD2 CLINVAR
OMIM 601366 CLINVAR