Variant #0000692454 (NC_000017.10:g.7123506G>A, NM_000018.3:c.128G>A (ACADVL))

Chromosome 17
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.7123506G>A
DNA change (hg38) -
Published as ACADVL(NM_000018.3):c.128G>A (p.(Gly43Asp))
ISCN -
DB-ID DLG4_000049
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) 0.03636 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 -?/. - c.128G>A r.(?) p.(Gly43Asp)
DLG4 NM_001365.3 -?/. - c.-1338C>T r.(?) p.(=)


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