Variant #0000259066 (NC_000017.10:g.8022065G>A, NM_001165960.1:c.32C>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.8022065G>A
DNA change (hg38) g.8118747G>A
Published as ALOXE3(NM_001165960.1):c.32C>T (p.P11L)
ISCN -
DB-ID ALOXE3_000004
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) 0.33461 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALOXE3 NM_001165960.1 -/. - c.32C>T r.(?) p.(Pro11Leu)
HES7 NM_001165967.1 -/. - c.*2824C>T r.(=) p.(=)
HES7 NM_032580.3 -/. - c.*2824C>T r.(=) p.(=)


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