Variant #0007486046 (NC_000011.9:g.77553559T>C, NM_024684.2:c.17T>C (AAMDC))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.77553559T>C
DB-ID -
dbSNP ID rs756810652
gnomAD frequency 1/245694
gnomAD homozygote count 0/122846
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     
AAMDC NM_024684.2 ./. c.17T>C r.(?) p.(Ile6Thr)