Variant #0000982754 (NC_000017.10:g.7106320G>A, NM_000018.3:c.-16984G>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.7106320G>A
DNA change (hg38) -
Published as DLG4(NM_001321075.3):c.689C>T (p.(Ala230Val))
ISCN -
DB-ID ACADVL_000076
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
ACADVL NM_000018.3 -?/. - c.-16984G>A r.(?) p.(=)
DLG4 NM_001365.3 -?/. - c.818C>T r.(?) p.(Ala273Val)


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