Variant #0000520547 (NC_000003.11:g.58491013_58491015del, NM_003500.3:c.1984_1986del (ACOX2))

Chromosome 3
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.58491013_58491015del
DNA change (hg38) g.58505286_58505288del
Published as ACOX2(NM_003500.4):c.1984_1986delGAG (p.E662del)
ISCN -
DB-ID ACOX2_000001
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACOX2 NM_003500.3 ?/. - c.1984_1986del r.(?) p.(Glu662del)
KCTD6 NM_153331.3 ?/. - c.*3654_*3656del r.(=) p.(=)


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