Variant #0000623768 (NC_000017.10:g.73956445C>T, NM_004035.6:c.281G>A (ACOX1))

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.73956445C>T
DNA change (hg38) g.75960364C>T
Published as ACOX1(NM_001185039.1):c.167G>A (p.R56Q)
ISCN -
DB-ID ACOX1_000014
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2025-01-07 15:52:25 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TEN1 NM_001113324.2 -?/. - c.-19154C>T r.(?) p.(=)
ACOX1 NM_004035.6 -?/. - c.281G>A r.(?) p.(Arg94Gln)


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