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
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
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
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

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