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Results for "PDE1B"

Variant Events: 3

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
PDE1B     DEASD_0237_002chr12:
54966430-54966430
GAexonicDe novononsynonymous SNVNM_001315535
NM_001165975
NM_001288769
NM_001315534
NM_000924
NM_001288768
c.G28A
c.G580A
c.G517A
c.G229A
c.G640A
c.G229A
p.G10S
p.G194S
p.G173S
p.G77S
p.G214S
p.G77S
32.0-DeRubeis2014 E
Kosmicki2017 E
Lim2017 E
PDE1B     SP0017232chr12:
54943667-54943667
CGexonicDe novononsynonymous SNVNM_000924c.C11Gp.S4C17.35-Feliciano2019 E
PDE1B     21854-36022chr12:
54955390-54955390
CTexonicInheritedstopgainNM_001165975c.C22Tp.Q8X37.00.001Callaghan2019 G
Source Variant Information

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Source:

Paper alias:

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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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