Variant #0012145621 (NC_000020.10:g.25281437G>T, NM_002862.3:c.*4279G>T (PYGB))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.25281437G>T
DB-ID -
dbSNP ID rs750402782
gnomAD frequency 1/245422
gnomAD homozygote count 0/122705
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD12 NM_001042472.2 ./. c.*44delCinsA r.(=) p.(=)
PYGB NM_002862.3 ./. c.*4279G>T r.(=) p.(=)