Variant #0001409378 (NC_000002.11:g.27353272T>C, NM_013388.4:c.*1010A>G (PREB))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.27353272T>C
DB-ID -
dbSNP ID rs202005994
gnomAD frequency 5/246216
gnomAD homozygote count 0/123102
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
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     
PREB NM_013388.4 ./. c.*1010A>G r.(=) p.(=)
ABHD1 NM_032604.3 ./. c.994delTinsC r.(?) p.(Ser332Pro)