Variant #0000520305 (NC_000003.11:g.52021376_52021379del, NM_000666.2:c.759_762del (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.52021376_52021379del
DNA change (hg38) g.51987360_51987363del
Published as ACY1(NM_000666.2):c.759_762delGACT (p.T254Sfs*2)
ISCN -
DB-ID ABHD14A_000005
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.759_762del r.(?) p.(Thr254SerfsTer2)
ABHD14A NM_015407.4 ?/. - c.*6342_*6345del r.(=) p.(=)
ABHD14A-ACY1 NR_037192.1 ?/. - n.1284_1287del r.(?) -


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