Variant #0000719531 (NC_000003.11:g.52022837C>T, NM_000666.2:c.1057C>T (ACY1))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.52022837C>T
DNA change (hg38) -
Published as ACY1(NM_000666.3):c.1057C>T (p.R353C)
ISCN -
DB-ID ABHD14A-ACY1_000002 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00266 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACY1 NM_000666.2 +/. - c.1057C>T r.(?) p.(Arg353Cys)
RPL29 NM_000992.2 +/. - c.*4928G>A r.(=) p.(=)
ABHD14A NM_015407.4 +/. - c.*7803C>T r.(=) p.(=)
ABHD14A-ACY1 NR_037192.1 +/. - n.1582C>T r.(?) -


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