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Results for "NIPAL3"

Variant Events: 9

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
NIPAL3     1-0495-003chr1:
24782317-24782317
CTintronicDe novo--Yuen2017 G
NIPAL3     Li2017:23082chr1:
24768672-24768672
CTexonicUnknownnonsynonymous SNVNM_020448c.C290Tp.A97V21.53.296E-5Li2017 T
NIPAL3     2-1114-003chr1:
24778791-24778791
AGintronicDe novo--Yuen2017 G
NIPAL3     Li2017:23041chr1:
24782657-24782657
GAexonicUnknownnonsynonymous SNVNM_020448c.G667Ap.V223M20.19.885E-5Li2017 T
NIPAL3     1-0567-004chr1:
24804670-24804670
AGintergenicDe novo--Yuen2017 G
NIPAL3     AU027506chr1:
24776653-24776653
GAintronicDe novo--Yuen2017 G
NIPAL3     Li2017:19723chr1:
24795644-24795644
AGexonicUnknownnonsynonymous SNVNM_020448c.A1190Gp.Y397C22.85.817E-5Li2017 T
NIPAL3     Li2017:15084chr1:
24795646-24795646
CTexonicUnknownstopgainNM_020448c.C1192Tp.R398X42.08.319E-6Li2017 T
NIPAL3     Li2017:16248chr1:
24776039-24776039
GAexonicUnknownnonsynonymous SNVNM_020448c.G463Ap.A155T28.31.648E-5Li2017 T
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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