Variant #0010491749 (NC_000017.10:g.35307676_35307677insT, NM_012138.3:c.256dupT (AATF))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.35307676_35307677insT
DB-ID -
dbSNP ID rs758427829
gnomAD frequency 1/246258
gnomAD homozygote count 0/123127
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AATF NM_012138.3 ./. c.256dupT r.(?) p.(Trp86LeufsTer10)