Variant #0003481597 (NC_000004.11:g.171009765A>C, NC_000004.11(NM_016228.3):c.68-50T>G (AADAT))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.171009765A>C
DB-ID -
dbSNP ID -
gnomAD frequency 1/242062
gnomAD homozygote count 0/121030
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     
AADAT NM_016228.3 ./. c.68-50T>G r.(=) p.(=)
AADAT NM_182662.1 ./. c.68-50T>G r.(=) p.(=)