Variant #0006403865 (NC_000010.10:g.255945C>T, NM_001202468.1:c.233C>T (ZMYND11))

Chromosome 10
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.255945C>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/246212
gnomAD homozygote count 0/123105
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     
ZMYND11 NM_001202464.1 ./. c.233C>T r.(?) p.(Ala78Val)
ZMYND11 NM_001202465.1 ./. c.233C>T r.(?) p.(Ala78Val)
ZMYND11 NM_001202466.1 ./. c.233C>T r.(?) p.(Ala78Val)
ZMYND11 NM_001202467.1 ./. c.233C>T r.(?) p.(Ala78Val)
ZMYND11 NM_001202468.1 ./. c.233C>T r.(?) p.(Ala78Val)
ZMYND11 NM_006624.5 ./. c.233C>T r.(?) p.(Ala78Val)
ZMYND11 NM_212479.3 ./. c.233C>T r.(?) p.(Ala78Val)