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Results for "RIMS4"

Variant Events: 7

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
RIMS4     1-0286-004chr20:
43391416-43391416
AGintronicDe novo--Yuen2017 G
RIMS4     SP0104002chr20:
43438793-43438793
TTGintronicDe novo--Fu2022 E
RIMS4     PN400137chr20:
43384973-43384973
GTexonicUnknown, De novostopgainNM_001205317
NM_182970
c.C615A
c.C612A
p.Y205X
p.Y204X
19.6-Leblond2019 E
Leblond2019 E
RIMS4     1-0224-004chr20:
43393050-43393050
CTintronicDe novo--Yuen2017 G
RIMS4     1-0113-003chr20:
43488595-43488595
GTintergenicDe novo--Yuen2016 G
RIMS4     1-0214-003chr20:
43420520-43420520
CAintronicDe novo--Yuen2017 G
RIMS4     2-0116-005chr20:
43447433-43447433
CAintergenicDe 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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