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Results for "ALOX12B"

Variant Events: 5

Gene
Gene symbol on which the variant is located
ID
Subject Identifier from the original study
Location
Genomic location of the reference allele
REF
Reference allele
ALT
Alternate allele
Context
Variant functional categories
Variant validation performed by an orthogonal method and reported
Inheritance
Reported inheritance status
Effects
Variant effect on transcript per Annovar
Transcript
Transcript used for the cDNA/Protein mutation
cDNA
cDNA variant notation
Protein
Protein variant notation
CADD-Phred v1.0
CADD phred-like score. This is phred-like rank score based on whole genome CADD raw scores
ExAC v0.3
ExAC population frequency (version 0.3)
Sources
Source(s) where variants from this event are reported
ALOX12B     1005chr17:
7974974-7974974
GAdownstreamDe novo--Trost2022 G
ALOX12B     SP0037348chr17:
7979691-7979691
CTintronicDe novo-1.0E-4Fu2022 E
Trost2022 G
ALOX12B     SP0008141chr17:
7989362-7989362
GAexonicDe novosynonymous SNVNM_001139c.C324Tp.Y108Y-9.0E-4Feliciano2019 E
Fu2022 E
Trost2022 G
Zhou2022 GE
ALOX12B     SP0071170chr17:
7990822-7990822
ATUTR5De novo--Fu2022 E
Trost2022 G
ALOX12B     10C102470chr17:
7983087-7983087
CTexonicDe novosynonymous SNVNM_001139c.G927Ap.E309E--DeRubeis2014 E
Fu2022 E
Kosmicki2017 E
Lim2017 E
Neale2012 E
Satterstrom2020 E
Trost2022 G
Zhou2022 GE
Source Variant Information

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Source:

Paper alias:

No records found.
Paper Information
Title
Authors
Technology
Variant source
Cohorts
Design
URL
Pubmed
Subject count
The number of subjects for this study could not be determined directly from the variant data; the value given is that reported by the authors in the publication.
Variant event count
Curation notesView
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