Variant #0012747747 (NC_000022.10:g.43089930_43089932del, NM_017436.4:c.26_28del (A4GALT))

Chromosome 22
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43089930_43089932del
DB-ID -
dbSNP ID rs760980696
gnomAD frequency 3/220390
gnomAD homozygote count 0/110187
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     
A4GALT NM_017436.4 ./. c.26_28del r.(?) p.(Leu9del)