Variant #0003025658 (NC_000004.11:g.466363C>A, NC_000004.11(NM_133474.3):c.34+1G>T (ZNF721))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.466363C>A
DB-ID -
dbSNP ID -
gnomAD frequency 1/242674
gnomAD homozygote count 0/121336
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     
ZNF721 NM_133474.3 ./. c.34+1G>T r.spl? p.?
ABCA11P NR_002451.2 ./. n.356+1G>T r.spl? p.?