Variant #0001029992 (NC_000012.11:g.121176429C>T, NM_000017.2:c.889C>T (ACADS))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.121176429C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ACADS_000020 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs747512252
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-03-19 13:28:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADS NM_000017.2 ?/. - c.889C>T r.(?) p.(Arg297Cys)


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