Variant #0000003903 (NC_000001.10:-, FH(NM_000143.3):c.-?_132+?del)

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type This mutation is novel, not a frequent cause of HLRCC syndrome. The mitochondrial signal peptide of
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID FH_00144
Frequency -
Variant remarks blood samples or cultured lymphocytes
ClassClinical -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FH NM_000143.3 ./. 01 c.-?_132+?del - -