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Results for "DPP4"

Variant Events: 11

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
DPP4     13409.p1chr2:
162865169-162865169
TCexonicDe novosynonymous SNVNM_001935c.A1890Gp.S630S--Iossifov2014 E
Kosmicki2017 E
O’Roak2012b E
Satterstrom2020 E
Trost2022 G
Wilfert2021 G
Zhou2022 GE
DPP4     AU3889305chr2:
162872465-162872465
GAintronicDe novo--Trost2022 G
Yuen2017 G
DPP4     5-0054-003chr2:
162940543-162940543
ACintergenicDe novo--Yuen2017 G
DPP4     13409_p1chr2:
162865169-162865169
TCexonicDe novosynonymous SNVNM_001935c.A1890Gp.S630S--Fu2022 E
DPP4     SP0024015chr2:
162930722-162930722
CTUTR5De novo--Fu2022 E
Trost2022 G
DPP4     4-0092-003chr2:
162865577-162865577
TCintronicDe novo--Trost2022 G
DPP4     MT_31.3chr2:
162918739-162918739
CCCTCAintronicDe novo--Trost2022 G
DPP4     1-1071-003chr2:
162850232-162850232
GAintronicDe novo--Trost2022 G
DPP4     MSSNG00222-003chr2:
162860873-162860873
CGintronicDe novo--Trost2022 G
DPP4     DEASD_0372_001chr2:
162891779-162891779
TTAexonicDe novoframeshift insertionNM_001935c.668dupTp.L223fs--DeRubeis2014 E
Fu2022 E
Kosmicki2017 E
Satterstrom2020 E
Trost2022 G
Zhou2022 GE
DPP4     SP0085811chr2:
162849921-162849921
ATintronicDe 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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