Variant #0000261761 (NC_000017.10:g.7120487C>T, NM_000018.3:c.-2817C>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.7120487C>T
DNA change (hg38) g.7217168C>T
Published as ACADVL(NM_001270447.1):c.23C>T (p.A8V)
ISCN -
DB-ID ACADVL_000069
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-11 16:12:30 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 -?/. - c.-2817C>T r.(?) p.(=)
DLG4 NM_001365.3 -?/. - c.159+1073G>A r.(=) p.(=)


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