or
or
Exact

Results for "UNC5A"

Variant Events: 12

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
UNC5A     PN400431chr5:
176306443-176306443
CTexonicUnknownnonsynonymous SNVNM_133369c.C2317Tp.R773W26.29.0E-4Leblond2019 E
UNC5A     SP0092935chr5:
176295320-176295320
TGintronicDe novo--Fu2022 E
UNC5A     1-0885-003chr5:
176302391-176302391
TCintronicDe novo--Trost2022 G
Yuen2017 G
UNC5A     SP0118178chr5:
176295826-176295826
GAexonicDe novosynonymous SNVNM_133369c.G582Ap.L194L5.312.519E-5Fu2022 E
Trost2022 G
Zhou2022 GE
UNC5A     SP0042850chr5:
176304794-176304794
GAintronicDe novo--Fu2022 E
UNC5A     1-0372-003chr5:
176271073-176271078
GGACGAGGAintronicDe novo--Yuen2017 G
UNC5A     AU1848302chr5:
176285803-176285803
GAintronicDe novo--Trost2022 G
UNC5A     3-0465-000chr5:
176292409-176292409
CTintronicDe novo--Trost2022 G
UNC5A     4-0085-003chr5:
176247474-176247474
TGintronicDe novo--Trost2022 G
UNC5A     3-0654-000chr5:
176273479-176273479
CTintronicDe novo--Trost2022 G
UNC5A     7-0012-003chr5:
176281736-176281736
TCintronicDe novo--Trost2022 G
Yuen2017 G
UNC5A     22124-39156chr5:
176295851-176295851
GAexonicInheritednonsynonymous SNVNM_133369c.G607Ap.E203K29.2-Callaghan2019 G
Source Variant Information

, -

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
More