RGD:408385414 Rat Genome Database

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Variant: RGD:408385414 -  Homo sapiens

RGD ID: 408385414
ClinVar ID: CV3527014
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GABBR2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 9 101,073,393
GRCh38 9 98,311,111
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_005458.8:c.1988A>G
NG_016426.1:g.403087A>G
NC_000009.12:g.98311111T>C
NC_000009.11:g.101073393T>C
More... 		01/17/2024 missense variant uncertain significance none provided

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Database
Acc Id
Source(s)
ClinVar RCV004772327 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GABBR2 CLINVAR
OMIM 607340 CLINVAR