Variant #0003203111 (NC_000004.11:g.57250350A>G, NM_181806.2:c.116T>C (AASDH))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.57250350A>G
DB-ID -
dbSNP ID rs770984557
gnomAD frequency 1/246228
gnomAD homozygote count 0/123113
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     
AASDH NM_181806.2 ./. c.116T>C r.(?) p.(Val39Ala)