Variant #0000016564 (NC_000017.10:g.7126103dup, ACADVL(NM_000018.3):c.996dup)

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type Duplication
DNA change (genomic) (Relative to hg19 / GRCh37) g.7126103dup
Reference -
DB-ID ACADVL_000042
Frequency 1/187
Variant remarks -
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner ting zhang
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ting zhang
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 +?/+? 10 c.996dup r.(?) p.(Ala333Cysfs*26)