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Results for "PHTF2"

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
PHTF2     13023.p1chr7:
77644281-77644281
CAintergenicDe novo--Turner2016 G
PHTF2     1-0300-003chr7:
77527584-77527584
CGintronicDe novo--Yuen2017 G
PHTF2     2-1235-004chr7:
77488065-77488065
AGintronicDe novo--Yuen2017 G
PHTF2     AU076704chr7:
77624227-77624227
GAintergenicDe novo--Yuen2017 G
PHTF2     1-0555-003chr7:
77525429-77525429
GGCTTAintronicDe novo--Yuen2017 G
PHTF2     AU3637301chr7:
77552094-77552094
AGexonicDe novononsynonymous SNVNM_020432
NM_001127357
NM_001127358
NM_001127359
NM_001127360
c.A1004G
c.A1016G
c.A1004G
c.A1016G
c.A1004G
p.E335G
p.E339G
p.E335G
p.E339G
p.E335G
26.5-Yuen2017 G
PHTF2     11003.p1chr7:
77572116-77572116
GAintronicMosaic--Dou2017 E
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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