Variant #0000258901 (NC_000017.10:g.73949540G>C, NM_004035.6:c.936C>G (ACOX1))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.73949540G>C
DNA change (hg38) g.75953459G>C
Published as ACOX1(NM_001185039.2):c.822C>G (p.I274M)
ISCN -
DB-ID ACOX1_000003
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) 0.65379 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
TEN1 NM_001113324.2 -/. - c.-26059G>C r.(?) p.(=)
ACOX1 NM_004035.6 -/. - c.936C>G r.(?) p.(Ile312Met)


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