RGD:407513433 Rat Genome Database

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Variant: RGD:407513433 -  Homo sapiens

RGD ID: 407513433
ClinVar ID: CV3461164
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PROM1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 16,035,069
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001145847.2:c.340A>T
NM_001145848.2:c.340A>T
NM_001145851.2:c.340A>T
NM_001145852.2:c.340A>T
More... 		06/19/2024 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004648822 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene PROM1 CLINVAR
OMIM 604365 CLINVAR