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Results for "RPS9"

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
RPS9     2-0122-003chr19:
54710232-54710232
GTexonicDe novononsynonymous SNVNM_001013c.G309Tp.E103D14.94-Trost2022 G
Yuen2015 G
Yuen2017 G
RPS9     SP0063295chr19:
54711343-54711343
GAexonicnonsynonymous SNVNM_001013c.G485Ap.R162H18.01-Zhou2022 GE
RPS9     7-0222-003chr19:
54718862-54718862
AGintergenicDe novo--Yuen2017 G
RPS9     REACH000001chr19:
54710671-54710671
GTintronicDe novo--Trost2022 G
RPS9     1-0649-003chr19:
54709582-54709582
GAintronicDe novo--Trost2022 G
RPS9     2-1178-003chr19:
54712881-54712881
CTintergenicDe novo--Yuen2016 G
Yuen2017 G
RPS9     SP0044098chr19:
54704841-54704841
ACintronicDe novo--Fu2022 E
Trost2022 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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