RGD:407516968 Rat Genome Database

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Variant: RGD:407516968 -  Homo sapiens

RGD ID: 407516968
ClinVar ID: CV3465935
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NRSN2  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 20 330,372
GRCh38 20 349,728
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001323679.2:c.85C>A
NM_001323680.2:c.85C>A
NM_001323681.2:c.85C>A
NM_001323682.2:c.85C>A
More... 		03/19/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004650471 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene NRSN2 CLINVAR
OMIM 610666 CLINVAR