RGD:407516718 Rat Genome Database

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Variant: RGD:407516718 -  Homo sapiens

RGD ID: 407516718
ClinVar ID: CV3465789
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NR2C1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 95,425,137
GRCh38 12 95,031,361
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001032287.3:c.1381A>G
NM_001127362.2:c.1381A>G
NM_003297.4:c.1381A>G
NC_000012.12:g.95031361T>C
More... 		05/29/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004650377 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene NR2C1 CLINVAR
OMIM 601529 CLINVAR