Variant #0000562937 (NC_000017.10:g.7123838C>T, NM_000018.3:c.194C>T (ACADVL))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7123838C>T
DNA change (hg38) g.7220519C>T
Published as ACADVL(NM_000018.4):c.194C>T (p.P65L)
ISCN -
DB-ID DLG4_000026
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) 0.008 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 -/. - c.194C>T r.(?) p.(Pro65Leu)
DLG4 NM_001365.3 -/. - c.-1670G>A r.(?) p.(=)
DVL2 NM_004422.2 -/. - c.*5346G>A r.(=) p.(=)


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