RGD:407492418 Rat Genome Database

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Variant: RGD:407492418 -  Homo sapiens

RGD ID: 407492418
ClinVar ID: CV3473591
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SERAC1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 158,567,925
GRCh38 6 158,146,893
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_032889.1:g.26388A>G
NC_000006.12:g.158146893T>C
NC_000006.11:g.158567925T>C
NR_073096.2:n.500A>G
More... 		03/16/2024 missense variant likely benign
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
CV3473591Humangenetic disease  IAGP 8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVar 


.


Database
Acc Id
Source(s)
ClinVar RCV004667119 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene SERAC1 CLINVAR
OMIM 614725 CLINVAR