Variant #0000003629 (NC_000017.10:-, ELAC2(NM_018127.6):c.646G>T)

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID ELAC2_00005
Frequency 2/3
Variant remarks This alteration was not present in

the one female available for study
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ELAC2 NM_018127.6 ./. 07 c.646G>T - p.Glu216X