Variant #0000517793 (NC_000003.11:g.128598491_128598494dup, NM_014049.4:c.-44_-41dup (ACAD9))

Chromosome 3
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.128598491_128598494dup
DNA change (hg38) g.128879648_128879651dup
Published as ACAD9(NM_014049.5):c.-44_-41dupTAAG, ACAD9(NR_033426.1):n.158_159insTAAG
ISCN -
DB-ID ACAD9_000030 See all 2 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACAD9 NM_014049.4 -?/. - c.-44_-41dup r.(?) p.(=)


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