RGD:407474279 Rat Genome Database

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Variant: RGD:407474279 -  Homo sapiens

RGD ID: 407474279
ClinVar ID: CV3424026
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BNC1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 83,933,156
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001301206.2:c.826C>T
NM_001717.4:c.847C>T
NC_000015.10:g.83264404G>A
NC_000015.9:g.83933156G>A
More... 		06/16/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004600574 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene BNC1 CLINVAR
OMIM 601930 CLINVAR