Variant #0005390317 (NC_000008.10:g.192891C>G, NM_001042415.1:c.17C>G (ZNF596))

Chromosome 8
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.192891C>G
DB-ID -
dbSNP ID rs368685119
gnomAD frequency 3/224522
gnomAD homozygote count 0/112257
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     
ZNF596 NM_001042415.1 ./. c.17C>G r.(?) p.(Ser6Cys)
ZNF596 NM_001042416.1 ./. c.17C>G r.(?) p.(Ser6Cys)
ZNF596 NM_173539.2 ./. c.17C>G r.(?) p.(Ser6Cys)