Variant #0007486047 (NC_000011.9:g.77553561G>C, NM_024684.2:c.19G>C (AAMDC))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.77553561G>C
DB-ID -
dbSNP ID rs781000871
gnomAD frequency 2/245754
gnomAD homozygote count 0/122875
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAMDC NM_024684.2 ./. c.19G>C r.(?) p.(Ala7Pro)