Variant #0000927671 (NC_000017.10:g.7125591T>C, NM_000018.3:c.848T>C (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.7125591T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ACADVL_000010 See all 14 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs113994167
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00128 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-05-24 13:25:01 +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.848T>C r.(?) p.(Val283Ala)


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