Variant #0000261787 (NC_000017.10:g.73969706C>T, NC_000017.10(NM_004035.6):c.269+4909G>A (ACOX1))

Chromosome 17
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.73969706C>T
DNA change (hg38) g.75973625C>T
Published as ACOX1(NM_007292.5):c.430G>A (p.G144R, p.(Gly144Arg))
ISCN -
DB-ID ACOX1_000004 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) 3.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TEN1 NM_001113324.2 ?/. - c.-5893C>T r.(?) p.(=)
ACOX1 NM_004035.6 ?/. - c.269+4909G>A r.(=) p.(=)


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