Variant #0005390327 (NC_000008.10:g.192912T>C, NM_001042415.1:c.38T>C (ZNF596))

Chromosome 8
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.192912T>C
DB-ID -
dbSNP ID rs759966957
gnomAD frequency 3/240430
gnomAD homozygote count 0/120212
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.38T>C r.(?) p.(Ile13Thr)
ZNF596 NM_001042416.1 ./. c.38T>C r.(?) p.(Ile13Thr)
ZNF596 NM_173539.2 ./. c.38T>C r.(?) p.(Ile13Thr)