Variant #0000993796 (NC_000003.11:g.52022837C>T, NM_000666.2:c.1057C>T (ACY1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.52022837C>T
DNA change (hg38) -
Published as ACY1(NM_000666.2):c.1057C>T (p.(Arg353Cys)), ACY1(NM_000666.3):c.1057C>T (p.R353C)
ISCN -
DB-ID ABHD14A-ACY1_000002 See all 3 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




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.(?) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.