Variant #0000894236 (NC_000017.10:g.7125608G>A, NM_000018.3:c.865G>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.7125608G>A
DNA change (hg38) -
Published as ACADVL(NM_000018.4):c.865G>A (p.G289R)
ISCN -
DB-ID ACADVL_000001 See all 2 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) 0.00011 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 2022-11-01 13:41:49 +01:00 (CET)
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.865G>A r.(?) p.(Gly289Arg)
DLG4 NM_001365.3 +/. - c.-3440C>T r.(?) p.(=)
DVL2 NM_004422.2 +/. - c.*3576C>T r.(=) p.(=)


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