Variant #0000801314 (NC_000003.11:g.52022794G>A, NM_000666.2:c.1014G>A (ACY1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52022794G>A
DNA change (hg38) -
Published as ACY1(NM_000666.2):c.1014G>A (p.L338=)
ISCN -
DB-ID ABHD14A_000013
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) 0.00042 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACY1 NM_000666.2 -?/. - c.1014G>A r.(?) p.(Leu338=)
RPL29 NM_000992.2 -?/. - c.*4971C>T r.(=) p.(=)
ABHD14A NM_015407.4 -?/. - c.*7760G>A r.(=) p.(=)
ABHD14A-ACY1 NR_037192.1 -?/. - n.1539G>A r.(?) -


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