Variant #0001055831 (NC_000017.10:g.8021431G>A, NM_001165960.1:c.274C>T (ALOXE3))

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.8021431G>A
DNA change (hg38) -
Published as ALOXE3(NM_001165960.1):c.274C>T (p.(Pro92Ser))
ISCN -
DB-ID ALOXE3_000027
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALOXE3 NM_001165960.1 ?/. - c.274C>T r.(?) p.(Pro92Ser)
HES7 NM_001165967.1 ?/. - c.*3458C>T r.(=) p.(=)
HES7 NM_032580.3 ?/. - c.*3458C>T r.(=) p.(=)


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