or
or
Exact

Results for "FNIP1"

Variant Events: 7

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
FNIP1     AU047703chr5:
131138772-131138772
GAintergenicDe novo--Yuen2017 G
FNIP1     10C104773chr5:
131013499-131013499
TCexonicDe novosynonymous SNVNM_001008738
NM_133372
c.A1332G
c.A1416G
p.P444P
p.P472P
--DeRubeis2014 E
Kosmicki2017 E
Lim2017 E
Neale2012 E
Satterstrom2020 E
FNIP1     1-0158-003chr5:
131039397-131039397
TCintronicDe novo--Yuen2017 G
FNIP1     AU3724302chr5:
131043336-131043336
GAintronicDe novo--Yuen2017 G
FNIP1     AU4173301chr5:
131058755-131058755
GAintronicDe novo--Yuen2017 G
FNIP1     2-1506-003chr5:
130982455-130982455
ACintronicDe novo--Yuen2017 G
FNIP1     13951.p1chr5:
131001561-131001561
CTintronicDe novo--Turner2016 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