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Results for "HIPK1"

Variant Events: 10

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
HIPK1     SP0118780chr1:
114499936-114499936
ACintronicDe novo--Fu2022 E
HIPK1     iHART1934chr1:
114512690-114512690
CTexonicMaternalstopgainNM_181358
NM_198269
NM_152696
NM_198268
c.C1702T
c.C1762T
c.C2884T
c.C2884T
p.R568X
p.R588X
p.R962X
p.R962X
19.28-Ruzzo2019 G
HIPK1     7-0461-003chr1:
114483469-114483469
CTexonicDe novononsynonymous SNVNM_152696
NM_198268
c.C464T
c.C464T
p.A155V
p.A155V
12.25-Trost2022 G
Zhou2022 GE
HIPK1     iHART1930chr1:
114512690-114512690
CTexonicMaternalstopgainNM_181358
NM_198269
NM_152696
NM_198268
c.C1702T
c.C1762T
c.C2884T
c.C2884T
p.R568X
p.R588X
p.R962X
p.R962X
19.28-Ruzzo2019 G
HIPK1     iHART1931chr1:
114512690-114512690
CTexonicMaternalstopgainNM_181358
NM_198269
NM_152696
NM_198268
c.C1702T
c.C1762T
c.C2884T
c.C2884T
p.R568X
p.R588X
p.R962X
p.R962X
19.28-Ruzzo2019 G
HIPK1     A59chr1:
114483086-114483086
GCexonicDe novononsynonymous SNVNM_152696
NM_198268
c.G81C
c.G81C
p.E27D
p.E27D
25.3-Jiao2019 E
HIPK1     mAGRE1934chr1:
114512690-114512690
CTexonicMaternalstopgainNM_181358
NM_198269
NM_152696
NM_198268
c.C1702T
c.C1762T
c.C2884T
c.C2884T
p.R568X
p.R588X
p.R962X
p.R962X
19.28-Cirnigliaro2023 G
HIPK1     mAGRE1931chr1:
114512690-114512690
CTexonicMaternalstopgainNM_181358
NM_198269
NM_152696
NM_198268
c.C1702T
c.C1762T
c.C2884T
c.C2884T
p.R568X
p.R588X
p.R962X
p.R962X
19.28-Cirnigliaro2023 G
HIPK1     mAGRE1930chr1:
114512690-114512690
CTexonicMaternalstopgainNM_181358
NM_198269
NM_152696
NM_198268
c.C1702T
c.C1762T
c.C2884T
c.C2884T
p.R568X
p.R588X
p.R962X
p.R962X
19.28-Cirnigliaro2023 G
HIPK1     1-0636-003chr1:
114472333-114472353
AGGCGGCGGCGGCGGCGGCGGAGGCGGCGGCGGCGGCGGintronicDe 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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