Variant #0000808241 (NC_000017.10:g.7123482del, NM_000018.3:c.104del (ACADVL))

Chromosome 17
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.7123482del
DNA change (hg38) -
Published as ACADVL(NM_000018.3):c.104delC (p.P35Lfs*26), ACADVL(NM_000018.4):c.104del (p.(Pro35Leufs*26))
ISCN -
DB-ID DLG4_000024 See all 4 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) 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 +/. - c.104del r.(?) p.(Pro35LeufsTer26)
DLG4 NM_001365.3 +/. - c.-1312del r.(?) p.(=)


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