Variant #0000562953 (NC_000017.10:g.7132774G>A, NM_000018.3:c.*4358G>A (ACADVL))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7132774G>A
DNA change (hg38) g.7229455G>A
Published as DVL2(NM_004422.2):c.748-8C>T (p.(=))
ISCN -
DB-ID DLG4_000037
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) 0.00015 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-03-09 11:45:42 +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.*4358G>A r.(=) p.(=)
DLG4 NM_001365.3 -?/. - c.-10606C>T r.(?) p.(=)
DVL2 NM_004422.2 -?/. - c.748-8C>T r.(=) p.(=)


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