Variant #0005220408 (NC_000007.13:g.121773748C>A, NM_005763.3:c.33G>T (AASS))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.121773748C>A
DB-ID -
dbSNP ID rs780915761
gnomAD frequency 8/246182
gnomAD homozygote count 1/123084
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     
AASS NM_005763.3 ./. c.33G>T r.(?) p.(Arg11Ser)