Variant #0002548333 (NC_000003.11:g.52012796T>C, NM_000666.2:c.-4828T>C (ACY1))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52012796T>C
DB-ID -
dbSNP ID rs549243887
gnomAD frequency 31/19046
gnomAD homozygote count 0/9492
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.-4828T>C r.(=) p.(=)
ABHD14B NM_001146314.1 ./. c.-4844A>G r.(=) p.(=)
ACY1 NM_001198895.1 ./. c.-4823T>C r.(=) p.(=)
ACY1 NM_001198896.1 ./. c.-4828T>C r.(=) p.(=)
ACY1 NM_001198897.1 ./. c.-4828T>C r.(=) p.(=)
ACY1 NM_001198898.1 ./. c.-4828T>C r.(=) p.(=)
ABHD14B NM_001254753.1 ./. c.-4719A>G r.(=) p.(=)
ABHD14B NM_032750.2 ./. c.-5038A>G r.(=) p.(=)