Variant #0005220387 (NC_000007.13:g.121773690C>G, NM_005763.3:c.91G>C (AASS))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.121773690C>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/246234
gnomAD homozygote count 0/123116
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.91G>C r.(?) p.(Glu31Gln)