Variant #0000726652 (NC_000017.10:g.7123945G>A, NM_000018.3:c.227G>A (ACADVL))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.7123945G>A
DNA change (hg38) -
Published as ACADVL(NM_000018.3):c.227G>A (p.G76E)
ISCN -
DB-ID DLG4_000055
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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.227G>A r.(?) p.(Gly76Glu)
DLG4 NM_001365.3 ?/. - c.-1777C>T r.(?) p.(=)
DVL2 NM_004422.2 ?/. - c.*5239C>T r.(=) p.(=)


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