Variant #0000563724 (NC_000017.10:g.7984260_7984263dup, NM_001139.2:c.467_470dup (ALOX12B))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7984260_7984263dup
DNA change (hg38) g.8080942_8080945dup
Published as ALOX12B(NM_001139.3):c.467_470dupATGT (p.H158Cfs*20)
ISCN -
DB-ID ALOX12B_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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ALOX12B NM_001139.2 +/. - c.467_470dup r.(?) p.(His158CysfsTer20)


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