RGD:405130766 Rat Genome Database

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Variant: RGD:405130766 -  Homo sapiens

RGD ID: 405130766
ClinVar ID: CV3115041
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOXC2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 16 86,601,984
GRCh38 16 86,568,378
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1292t1:c.1043T>C
NM_005251.3:c.1043T>C
LRG_1292:g.6550T>C
NG_012025.2:g.6550T>C
More... 		09/13/2023 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003815886 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FOXC2 CLINVAR
OMIM 602402 CLINVAR