Variant #0000259065 (NC_000017.10:g.7999957G>A, NM_001165960.1:c.2520C>T (ALOXE3))

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.7999957G>A
DNA change (hg38) g.8096639G>A
Published as ALOXE3(NM_001165960.1):c.2520C>T (p.S840=)
ISCN -
DB-ID ALOXE3_000001 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) 0.4592 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 2020-07-11 16:07:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALOXE3 NM_001165960.1 -/. - c.2520C>T r.(?) p.(Ser840=)


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