RGD:150477609 Rat Genome Database

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Variant: RGD:150477609 -  Homo sapiens

RGD ID: 150477609
RS ID: rs142499350
ClinVar ID: CV1240055
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NR2F2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 96,875,270
GRCh38 15 96,332,041
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021005.4:c.-65C>T
NM_001145155.2:c.44-2035C>T
NG_016753.1:g.11114C>T
NC_000015.10:g.96332041C>T
More... 		06/20/2021 5 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NR2F2
Accession:NM_021005
Location:5UTRS;EXON

Gene Symbol:NR2F2
Accession:NM_001145155
Location:INTRON

Gene Symbol:NR2F2
Accession:NM_001145157
Location:INTRON

Gene Symbol:NR2F2
Accession:NM_001145156
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001652233 CLINVAR
dbSNP (RS) rs142499350 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NR2F2 CLINVAR
OMIM 107773 CLINVAR