RGD:408391705 Rat Genome Database

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Variant: RGD:408391705 -  Homo sapiens

RGD ID: 408391705
ClinVar ID: CV3523332
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GJB3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 35,250,664
GRCh38 1 34,785,063
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001005752.2:c.301C>T
NM_024009.3:c.301C>T
NG_008309.1:g.8875C>T
NC_000001.11:g.34785063C>T
More... 		11/10/2023 missense variant uncertain significance none provided

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Database
Acc Id
Source(s)
ClinVar RCV004770705 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GJB3 CLINVAR
OMIM 603324 CLINVAR