Variant #0012048827 (NC_000020.10:g.76771C>T, NM_153325.2:c.184C>T (DEFB125))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.76771C>T
DB-ID -
dbSNP ID rs41276376
gnomAD frequency 332/246192
gnomAD homozygote count 0/122764
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     
DEFB125 NM_153325.2 ./. c.184C>T r.(?) p.(His62Tyr)