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Results for "RBMXL3"

Variant Events: 6

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
RBMXL3     REACH000089chrX:
114425125-114425125
GCexonicnonsynonymous SNVNM_001145346c.G1121Cp.S374T5.542-Zhou2022 GE
RBMXL3     74-0358chrX:
114424585-114424585
TGexonicInheritednonsynonymous SNVNM_001145346c.T581Gp.L194W10.25-Patowary2019 E
RBMXL3     2-1737-003chrX:
114426333-114426333
GTexonicDe novononsynonymous SNVNM_001145346c.G2329Tp.G777C7.236-Yuen2017 G
Zhou2022 GE
RBMXL3     AU2363301chrX:
114424940-114424940
CTexonicsynonymous SNVNM_001145346c.C936Tp.G312G-2.0E-4Zhou2022 GE
RBMXL3     mAGRE2016chrX:
114424362-114424362
CTexonicUnknownstopgainNM_001145346c.C358Tp.R120X14.86-Cirnigliaro2023 G
RBMXL3     mAGRE2390chrX:
114424223-114424223
CAexonicUnknownstopgainNM_001145346c.C219Ap.Y73X13.08-Cirnigliaro2023 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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