Variant #0000982769 (NC_000017.10:g.7127184G>A, NM_000018.3:c.1322G>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.7127184G>A
DNA change (hg38) -
Published as ACADVL(NM_000018.4):c.1322G>A (p.(Gly441Asp))
ISCN -
DB-ID ACADVL_000004 See all 5 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) 2.0E-5 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 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.1322G>A r.(?) p.(Gly441Asp)
DLG4 NM_001365.3 +/. - c.-5016C>T r.(?) p.(=)
DVL2 NM_004422.2 +/. - c.*2000C>T r.(=) p.(=)


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