RGD:11545479 Rat Genome Database

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Variant: RGD:11545479 -  Homo sapiens

RGD ID: 11545479
RS ID: rs145924266
ClinVar ID: CV250963
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FOXL2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 138,665,815
GRCh38 3 138,946,973
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012454.1:g.5168G>A
NC_000003.12:g.138946973C>T
NC_000003.11:g.138665815C>T
LRG_1295:g.5168G>A
More... 		5 prime utr variant benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:FOXL2
Accession:NM_023067
Location:5UTRS;EXON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000245190 CLINVAR
dbSNP (RS) rs145924266 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene FOXL2 CLINVAR
OMIM 605597 CLINVAR