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Results for "GTF2IRD1"

Variant Events: 31

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
GTF2IRD1     1-1006-003Achr7:
74014616-74014616
CTintronicDe novo--Trost2022 G
GTF2IRD1     7-0011-003chr7:
73974827-73974830
ATATAintronicDe novo--Trost2022 G
GTF2IRD1     1-1018-003chr7:
73969803-73969803
CAexonicDe novononsynonymous SNVNM_001199207
NM_005685
NM_016328
c.C2098A
c.C2002A
c.C2047A
p.L700M
p.L668M
p.L683M
11.0-Trost2022 G
Zhou2022 GE
GTF2IRD1     5-0097-003chr7:
73976685-73976685
GAintronicDe novo--Trost2022 G
GTF2IRD1     MSSNG00167-003chr7:
73935693-73935693
GAintronicDe novo--Trost2022 G
GTF2IRD1     SP0114923chr7:
73961410-73961410
CTintronicDe novo--Trost2022 G
GTF2IRD1     SP0005363chr7:
73922598-73922598
ACintronicDe novo--Trost2022 G
GTF2IRD1     2-1733-003chr7:
73923424-73923424
CTintronicDe novo--Trost2022 G
GTF2IRD1     AU3712302chr7:
73907341-73907341
GAintronicDe novo--Yuen2017 G
GTF2IRD1     2-0063-003chr7:
73916573-73916573
ATintronicDe novo--Trost2022 G
Yuen2017 G
GTF2IRD1     2-0273-003chr7:
74014944-74014944
AGintronicDe novo--Trost2022 G
Yuen2017 G
GTF2IRD1     1-0673-003chr7:
73886674-73886674
ATintronicDe novo--Trost2022 G
Yuen2017 G
GTF2IRD1     2-0122-003chr7:
73896807-73896807
CTintronicDe novo--Trost2022 G
Yuen2017 G
GTF2IRD1     AU3586303chr7:
73932144-73932144
CGintronicDe novo--Yuen2017 G
GTF2IRD1     2-1375-003chr7:
74037292-74037292
GCintergenicDe novo--Yuen2016 G
Yuen2017 G
GTF2IRD1     AU3779302chr7:
74005204-74005204
CTexonicDe novononsynonymous SNVNM_001199207
NM_005685
NM_016328
c.C2545T
c.C2449T
c.C2494T
p.R849W
p.R817W
p.R832W
21.0-Trost2022 G
Yuen2017 G
Zhou2022 GE
GTF2IRD1     7-0148-003chr7:
73951009-73951009
AGintronicDe novo--Trost2022 G
Yuen2017 G
GTF2IRD1     SP0005107chr7:
73952519-73952519
GTintronicDe novo-1.653E-5Fu2022 E
Trost2022 G
GTF2IRD1     SP0139196chr7:
73949381-73949381
CTintronicDe novo--Fu2022 E
GTF2IRD1     AU3636302chr7:
73910499-73910499
GAintronicDe novo--Trost2022 G
Yuen2017 G
GTF2IRD1     4-0062-003chr7:
73913163-73913164
ATCCintronicDe novo--Trost2022 G
GTF2IRD1     12295.p1chr7:
73969529-73969529
AGexonicDe novononsynonymous SNVNM_001199207
NM_005685
NM_016328
c.A2038G
c.A1942G
c.A1942G
p.K680E
p.K648E
p.K648E
12.898.271E-6Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Sanders2012 E
Satterstrom2020 E
Zhou2022 GE
GTF2IRD1     4-0062-003chr7:
73913172-73913172
CAintronicDe novo--Trost2022 G
GTF2IRD1     7-0121-003chr7:
73897126-73897126
CTintronicDe novo--Trost2022 G
GTF2IRD1     AU061003chr7:
73909852-73909852
CTintronicDe novo--Trost2022 G
GTF2IRD1     1-1186-003chr7:
73890327-73890327
CTintronicDe novo--Trost2022 G
GTF2IRD1     SP0085417chr7:
73959021-73959021
GAintronicDe novo--Fu2022 E
GTF2IRD1     AU2770301chr7:
73892909-73892909
CAintronicDe novo--Trost2022 G
GTF2IRD1     GEA331chr7:
74015575-74015575
CTintronicDe novo12.57-Fu2022 E
GTF2IRD1     SSC04105chr7:
73969529-73969529
AGexonicDe novononsynonymous SNVNM_001199207
NM_005685
NM_016328
c.A2038G
c.A1942G
c.A1942G
p.K680E
p.K648E
p.K648E
12.898.271E-6Fu2022 E
Trost2022 G
GTF2IRD1     SJD_46.3chr7:
73887444-73887444
CGintronicDe novo--Trost2022 G
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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