RGD:405199492 Rat Genome Database

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Variant: RGD:405199492 -  Homo sapiens

RGD ID: 405199492
ClinVar ID: CV3128828
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RET  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 43,607,547
GRCh38 10 43,112,099
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_518t1:c.1523A>T
LRG_518t2:c.1523A>T
NM_001406771.1:c.1085A>T
NM_001406773.1:c.1085A>T
More... 		03/04/2023 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003821871 CLINVAR
MedGen C4048306 CLINVAR
NCBI Gene RET CLINVAR
OMIM 164761 CLINVAR
SNOMED CT 61808009 CLINVAR