Variant #0001066606 (NC_000017.10:g.7125591T>C, NM_000018.3:c.848T>C (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.7125591T>C
DNA change (hg38) -
Published as ACADVL(NM_001270448.1):c.620T>C (p.V207A)
ISCN -
DB-ID ACADVL_000010 See all 15 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) 0.00128 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 +/. - c.848T>C r.(?) p.(Val283Ala)
DLG4 NM_001365.3 +/. - c.-3423A>G r.(?) p.(=)
DVL2 NM_004422.2 +/. - c.*3593A>G r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.