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Results for "CYP4F3"

Variant Events: 8

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
CYP4F3     mAGRE1714chr19:
15760747-15760749
CATCexonicMaternalframeshift deletionNM_000896
NM_001199208
NM_001199209
c.673_674del
c.673_674del
c.673_674del
p.I225fs
p.I225fs
p.I225fs
-3.295E-5Cirnigliaro2023 G
CYP4F3     12228.p1chr19:
15763419-15763419
CTexonicDe novononsynonymous SNVNM_000896
NM_001199208
NM_001199209
c.C959T
c.C959T
c.C959T
p.A320V
p.A320V
p.A320V
23.0-Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Sanders2012 E
Zhou2022 GE
CYP4F3     09C87503chr19:
15770161-15770161
GAexonicDe novononsynonymous SNVNM_000896
NM_001199208
NM_001199209
c.G1529A
c.G1529A
c.G1529A
p.G510D
p.G510D
p.G510D
10.58-Fu2022 E
CYP4F3     mAGRE1713chr19:
15760747-15760749
CATCexonicMaternalframeshift deletionNM_000896
NM_001199208
NM_001199209
c.673_674del
c.673_674del
c.673_674del
p.I225fs
p.I225fs
p.I225fs
-3.295E-5Cirnigliaro2023 G
CYP4F3     AU2427303chr19:
15760747-15760749
CATCexonicMaternalframeshift deletionNM_000896
NM_001199208
NM_001199209
c.673_674del
c.673_674del
c.673_674del
p.I225fs
p.I225fs
p.I225fs
-3.295E-5Cirnigliaro2023 G
CYP4F3     AU2427302chr19:
15760747-15760749
CATCexonicMaternalframeshift deletionNM_000896
NM_001199208
NM_001199209
c.673_674del
c.673_674del
c.673_674del
p.I225fs
p.I225fs
p.I225fs
-3.295E-5Cirnigliaro2023 G
CYP4F3     AU2427301chr19:
15760747-15760749
CATCexonicMaternalframeshift deletionNM_000896
NM_001199208
NM_001199209
c.673_674del
c.673_674del
c.673_674del
p.I225fs
p.I225fs
p.I225fs
-3.295E-5Cirnigliaro2023 G
CYP4F3     SP0062333chr19:
15769628-15769628
GAintronicDe novo--Fu2022 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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