Variant #0000563762 (NC_000017.10:g.8021612C>A, NM_001165960.1:c.93G>T (ALOXE3))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.8021612C>A
DNA change (hg38) g.8118294C>A
Published as ALOXE3(NM_001165960.1):c.93G>T (p.(Gln31His))
ISCN -
DB-ID ALOXE3_000012
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) 0.00587 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALOXE3 NM_001165960.1 -?/. - c.93G>T r.(?) p.(Gln31His)
HES7 NM_001165967.1 -?/. - c.*3277G>T r.(=) p.(=)
HES7 NM_032580.3 -?/. - c.*3277G>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.