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Results for "PDCD11"

Variant Events: 20

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
PDCD11     SP0001808chr10:
105205111-105205111
TCintronicDe novo--Fu2022 E
PDCD11     14643.p1chr10:
105184868-105184868
GAexonicDe novononsynonymous SNVNM_014976c.G2891Ap.R964H13.846.59E-5Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Krupp2017 E
Satterstrom2020 E
Wilfert2021 G
Zhou2022 GE
PDCD11     SP0123550chr10:
105197838-105197838
TGintronicDe novo--Fu2022 E
PDCD11     SP0022102chr10:
105183373-105183373
CTexonicDe novosynonymous SNVNM_014976c.C2721Tp.H907H-9.887E-5Fu2022 E
Trost2022 G
Zhou2022 GE
PDCD11     37086chr10:
105184868-105184868
GAexonicDe novononsynonymous SNVNM_014976c.G2891Ap.R964H13.846.59E-5Fu2022 E
Trost2022 G
PDCD11     SP0010834chr10:
105187162-105187162
TGintronicDe novo--Fu2022 E
Trost2022 G
PDCD11     SP0029524chr10:
105179261-105179261
CGintronicDe novo--Fu2022 E
PDCD11     Cukier2014:7435chr10:
105202091-105202091
GTexonicUnknownnonsynonymous SNVNM_014976c.G4829Tp.R1610L22.50.0018Cukier2014 E
PDCD11     AU3154302chr10:
105168731-105168731
CTintronicDe novo--Trost2022 G
Yuen2017 G
PDCD11     2-1355-004chr10:
105158109-105158109
TAintronicDe novo--Trost2022 G
Yuen2017 G
PDCD11     12208.p1chr10:
105160315-105160315
AGintronicDe novo-4.122E-5Satterstrom2020 E
Trost2022 G
PDCD11     MSSNG00066-003chr10:
105204981-105204981
GCintronicDe novo--Trost2022 G
PDCD11     14-1011chr10:
105201636-105201636
CTexonicDe novosynonymous SNVNM_014976c.C4611Tp.F1537F-2.473E-5Trost2022 G
Zhou2022 GE
PDCD11     2-1635-004chr10:
105201953-105201953
TGintronicDe novo--Trost2022 G
Yuen2017 G
PDCD11     SP0138633chr10:
105193754-105193754
GAexonicDe novononsynonymous SNVNM_014976c.G3524Ap.R1175Q26.09.0E-4Trost2022 G
PDCD11     SP0222356chr10:
105194651-105194651
TAexonicDe novononsynonymous SNVNM_014976c.T3764Ap.I1255K10.87-Trost2022 G
PDCD11     SP0028985chr10:
105181343-105181343
ATintronicDe novo--Trost2022 G
PDCD11     MSSNG00014-004chr10:
105182565-105182565
GAintronicDe novo--Trost2022 G
PDCD11     1-0359-003chr10:
105168393-105168393
GAintronicDe novo--Trost2022 G
Yuen2017 G
PDCD11     REACH000495chr10:
105187142-105187142
GAexonicnonsynonymous SNVNM_014976c.G3362Ap.R1121Q24.38.36E-6Zhou2022 GE
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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