Variant #0000002654 (NC_000001.10:-, CDC73(NM_024529.4):c.664C>T)

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Exon
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID CDC73_00039 See all 3 reported entries
Frequency -
Variant remarks The altered expression of parafibromin caused by HRPT2 gene mutation is one of the molecular mechanisms for explaining the clinical manifestations of this patient.
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDC73 NM_024529.4 ./. 07 c.664C>T - p.Arg222X