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Results for "ZBTB45"

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
ZBTB45     SP0059140chr19:
59028665-59028665
GAexonicDe novostopgainNM_001316978
NM_001316979
NM_001316980
NM_001316981
NM_001316982
NM_032792
c.C376T
c.C376T
c.C376T
c.C376T
c.C376T
c.C376T
p.R126X
p.R126X
p.R126X
p.R126X
p.R126X
p.R126X
19.549.935E-6Fu2022 E
Trost2022 G
Zhou2022 GE
ZBTB45     SSC10729chr19:
59028431-59028433
CAGCexonicDe novoframeshift deletionNM_001316978
NM_001316979
NM_001316980
NM_001316981
NM_001316982
NM_032792
c.608_609del
c.608_609del
c.608_609del
c.608_609del
c.608_609del
c.608_609del
p.P203fs
p.P203fs
p.P203fs
p.P203fs
p.P203fs
p.P203fs
--Fu2022 E
Trost2022 G
ZBTB45     SP0057248chr19:
59028593-59028593
GAexonicDe novononsynonymous SNVNM_001316978
NM_001316979
NM_001316980
NM_001316981
NM_001316982
NM_032792
c.C448T
c.C448T
c.C448T
c.C448T
c.C448T
c.C448T
p.R150C
p.R150C
p.R150C
p.R150C
p.R150C
p.R150C
16.65-Fu2022 E
Trost2022 G
Zhou2022 GE
ZBTB45     11511.p1chr19:
59028486-59028489
TGGGTexonicDe novononframeshift deletionNM_001316978
NM_001316979
NM_001316980
NM_001316981
NM_001316982
NM_032792
c.552_554del
c.552_554del
c.552_554del
c.552_554del
c.552_554del
c.552_554del
p.184_185del
p.184_185del
p.184_185del
p.184_185del
p.184_185del
p.184_185del
--Iossifov2014 E
Kosmicki2017 E
Satterstrom2020 E
Zhou2022 GE
ZBTB45     SP0108603chr19:
59025444-59025444
GTexonicDe novononsynonymous SNVNM_001316978
NM_001316979
NM_001316980
NM_001316981
NM_001316982
NM_032792
c.C1513A
c.C1513A
c.C1513A
c.C1513A
c.C1513A
c.C1513A
p.L505M
p.L505M
p.L505M
p.L505M
p.L505M
p.L505M
12.95-Fu2022 E
Trost2022 G
Zhou2022 GE
ZBTB45     AU083003chr19:
59025465-59025465
GAexonicUnknownnonsynonymous SNVNM_001316978
NM_001316979
NM_001316980
NM_001316981
NM_001316982
NM_032792
c.C1492T
c.C1492T
c.C1492T
c.C1492T
c.C1492T
c.C1492T
p.R498C
p.R498C
p.R498C
p.R498C
p.R498C
p.R498C
19.1-Stessman2017 T
ZBTB45     1-0755-003chr19:
59034053-59034053
GAintronicDe novo--Trost2022 G
Yuen2017 G
ZBTB45     3-0438-000chr19:
59050453-59050453
AGintronicDe novo--Trost2022 G
ZBTB45     31708chr19:
59028486-59028489
TGGGTexonicDe novononframeshift deletionNM_001316978
NM_001316979
NM_001316980
NM_001316981
NM_001316982
NM_032792
c.552_554del
c.552_554del
c.552_554del
c.552_554del
c.552_554del
c.552_554del
p.184_185del
p.184_185del
p.184_185del
p.184_185del
p.184_185del
p.184_185del
--Trost2022 G
ZBTB45     1-0214-003chr19:
59029098-59029098
AGintronicDe novo--Trost2022 G
Yuen2017 G
ZBTB45     14231.p1chr19:
59028431-59028433
CAGCexonicDe novoframeshift deletionNM_001316978
NM_001316979
NM_001316980
NM_001316981
NM_001316982
NM_032792
c.608_609del
c.608_609del
c.608_609del
c.608_609del
c.608_609del
c.608_609del
p.P203fs
p.P203fs
p.P203fs
p.P203fs
p.P203fs
p.P203fs
--Ji2016 E
Krumm2015 E
Satterstrom2020 E
Zhou2022 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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