Variant #0002548316 (NC_000003.11:g.52012378C>T, NM_000666.2:c.-5246C>T (ACY1))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52012378C>T
DB-ID -
dbSNP ID -
gnomAD frequency 4/150170
gnomAD homozygote count 0/75081
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     
ACY1 NM_000666.2 ./. c.-5246C>T r.(=) p.(=)
ABHD14B NM_001146314.1 ./. c.-4426G>A r.(=) p.(=)
ACY1 NM_001198895.1 ./. c.-5241C>T r.(=) p.(=)
ACY1 NM_001198896.1 ./. c.-5246C>T r.(=) p.(=)
ACY1 NM_001198897.1 ./. c.-5246C>T r.(=) p.(=)
ACY1 NM_001198898.1 ./. c.-5246C>T r.(=) p.(=)
ABHD14B NM_001254753.1 ./. c.-4301G>A r.(=) p.(=)
ABHD14A NM_015407.4 ./. c.385C>T r.(?) p.(Leu129Phe)
ABHD14B NM_032750.2 ./. c.-4620G>A r.(=) p.(=)