Variant #0000562916 (NC_000017.10:g.7099645G>A, NM_000018.3:c.-23659G>A (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.7099645G>A
DNA change (hg38) g.7196326G>A
Published as DLG4(NM_001365.4):c.1324C>T (p.R442*)
ISCN -
DB-ID DLG4_000022 See all 5 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-06-07 02:03:25 +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.-23659G>A r.(?) p.(=)
DLG4 NM_001365.3 +/. - c.1324C>T r.(?) p.(Arg442Ter)


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