Variant #0000325628 (NC_000017.10:g.73969777T>C, NC_000017.10(NM_004035.6):c.269+4838A>G (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.73969777T>C
DNA change (hg38) g.75973696T>C
Published as ACOX1(NM_001185039.1):c.155+4838A>G (p.(=))
ISCN -
DB-ID ACOX1_000005
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.-5822T>C r.(?) p.(=)
ACOX1 NM_004035.6 ?/. - c.269+4838A>G r.(=) p.(=)


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