Variant #0000801313 (NC_000003.11:g.52020669dup, NM_000666.2:c.575dup (ACY1))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.52020669dup
DNA change (hg38) -
Published as ACY1(NM_000666.3):c.575dupG (p.S192Rfs*64)
ISCN -
DB-ID ABHD14A_000012
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACY1 NM_000666.2 ?/. - c.575dup r.(?) p.(Ser192Argfs*64)
ABHD14A NM_015407.4 ?/. - c.*5635dup r.(?) p.(=)
ABHD14A-ACY1 NR_037192.1 ?/. - n.1100dup r.(?) -


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