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Results for "CAMK2B"

Variant Events: 25

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
CAMK2B     1-0763-003chr7:
44368303-44368303
GGGTAintergenicDe novo--Yuen2017 G
CAMK2B     2-0272-003chr7:
44294291-44294291
TCintronicDe novo--Yuen2017 G
CAMK2B     2-1382-003chr7:
44298128-44298128
CAintronicDe novo--Yuen2016 G
Yuen2017 G
CAMK2B     1-0541-003chr7:
44368286-44368286
AATGCTGGintergenicDe novo--Yuen2017 G
CAMK2B     SP0093105chr7:
44274315-44274315
CTintronicDe novo-1.698E-5Fu2022 E
CAMK2B     2-1170-003chr7:
44294312-44294312
CCCACCACCACCACCACCAintronicDe novo--Yuen2017 G
CAMK2B     Krgovic2022:035442chr7:
44294154-44294154
CTexonicUnknownnonsynonymous SNVNM_001220
NM_001293170
NM_172078
NM_172079
NM_172080
NM_172081
NM_172082
NM_172083
NM_172084
c.G328A
c.G328A
c.G328A
c.G328A
c.G328A
c.G328A
c.G328A
c.G328A
c.G328A
p.E110K
p.E110K
p.E110K
p.E110K
p.E110K
p.E110K
p.E110K
p.E110K
p.E110K
26.3-Krgovic2022 E
CAMK2B     2-0208-003chr7:
44368286-44368286
AATAGTGTintergenicDe novo--Yuen2017 G
CAMK2B     1-0435-003chr7:
44360225-44360225
CAintronicDe novo--Yuen2017 G
CAMK2B     SP0144117chr7:
44282824-44282824
CTintronicDe novo--Fu2022 E
CAMK2B     AU045514chr7:
44420898-44420904
CAGAGAGCAGAGintergenicDe novo--Yuen2017 G
CAMK2B     2-1508-004chr7:
44294312-44294312
CCCAintronicDe novo--Yuen2017 G
CAMK2B     1-0043-003chr7:
44294269-44294269
TAintronicDe novo--Yuen2017 G
CAMK2B     1-0104-003chr7:
44368283-44368283
AATAGTGTTGGTGGintergenicDe novo--Yuen2017 G
CAMK2B     SP0023236 Complex Event; expand row to view variants  De novononsynonymous SNVNM_001220
NM_001293170
NM_172078
NM_172079
NM_172080
NM_172081
NM_172082
NM_172083
NM_172084
NM_001220
NM_001293170
NM_172078
NM_172079
NM_172080
NM_172081
NM_172082
NM_172083
NM_172084
c.C199T
c.C199T
c.C199T
c.C199T
c.C199T
c.C199T
c.C199T
c.C199T
c.C199T
c.T200A
c.T200A
c.T200A
c.T200A
c.T200A
c.T200A
c.T200A
c.T200A
c.T200A
p.L67F
p.L67F
p.L67F
p.L67F
p.L67F
p.L67F
p.L67F
p.L67F
p.L67F
p.L67H
p.L67H
p.L67H
p.L67H
p.L67H
p.L67H
p.L67H
p.L67H
p.L67H
23.0-Antaki2022 GE
Antaki2022 GE
Fu2022 E
CAMK2B     JASD_Fam0070chr7:
44259671-44259671
GAexonicDe novononsynonymous SNVNM_172084
NM_172083
NM_172081
NM_172079
NM_172080
NM_172082
NM_001293170
NM_172078
NM_001220
c.C1340T
c.C1430T
c.C1502T
c.C1547T
c.C1544T
c.C1469T
c.C1619T
c.C1619T
c.C1991T
p.P447L
p.P477L
p.P501L
p.P516L
p.P515L
p.P490L
p.P540L
p.P540L
p.P664L
29.6-Takata2018 E
CAMK2B     2-0088-003chr7:
44368294-44368294
GGGTGGTGGTAATGGTGGTGGTGGTAATGGTGGTGGTGGTAintergenicDe novo--Yuen2017 G
CAMK2B     AU3779304chr7:
44415521-44415521
TCintergenicDe novo--Yuen2017 G
CAMK2B     1-0508-003chr7:
44264287-44264287
GAintronicDe novo--Yuen2017 G
CAMK2B     2-1169-004chr7:
44267564-44267564
AGintronicDe novo--Yuen2017 G
CAMK2B     AU4154303chr7:
44306328-44306328
GAintronicDe novo--Yuen2017 G
CAMK2B     PN400439chr7:
44269056-44269056
CTexonicUnknownnonsynonymous SNVNM_001220c.G1270Ap.G424R21.2-Leblond2019 E
CAMK2B     1-0473-003chr7:
44368286-44368286
AATAATGATAATGATAGTGTintergenicDe novo--Yuen2017 G
CAMK2B     152311chr7:
44268358-44268358
GAintronicDe novo-2.0E-4Satterstrom2020 E
CAMK2B     AU3790302chr7:
44297033-44297033
CAintronicDe novo--Yuen2017 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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