Variant #0000562939 (NC_000017.10:g.7124859C>T, NM_000018.3:c.480C>T (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.7124859C>T
DNA change (hg38) g.7221540C>T
Published as ACADVL(NM_001270448.1):c.252C>T (p.Y84=)
ISCN -
DB-ID DLG4_000028
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) 4.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-06-09 07:58:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 -?/. - c.480C>T r.(?) p.(Tyr160=)
DLG4 NM_001365.3 -?/. - c.-2691G>A r.(?) p.(=)
DVL2 NM_004422.2 -?/. - c.*4325G>A r.(=) p.(=)


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