RGD:597652679 Rat Genome Database

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Variant: RGD:597652679 -  Homo sapiens

RGD ID: 597652679
ClinVar ID: CV3555409
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NAALAD2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 89,902,143
GRCh38 11 90,168,975
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001300930.2:c.1226C>T
NM_005467.4:c.1325C>T
NC_000011.10:g.90168975C>T
NC_000011.9:g.89902143C>T
More... 		10/12/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004833852 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene NAALAD2 CLINVAR
OMIM 611636 CLINVAR