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Results for "SNRNP200"

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
SNRNP200     13026.p1chr2:
96953160-96953160
GAintronicDe novo-1.647E-5Iossifov2014 E
Kosmicki2017 E
Satterstrom2020 E
SNRNP200     DEASD_0008_001chr2:
96962741-96962741
TCexonicDe novononsynonymous SNVNM_014014c.A1445Gp.N482S26.1-DeRubeis2014 E
Kosmicki2017 E
Lim2017 E
Satterstrom2020 E
SNRNP200     AU0786305chr2:
96969006-96969006
GAexonicDe novononsynonymous SNVNM_014014c.C272Tp.S91L14.888.236E-6Yuen2017 G
SNRNP200     3-0216-000chr2:
96964038-96964038
TCexonicDe novononsynonymous SNVNM_014014c.A1103Gp.K368R13.27-Yuen2017 G
SNRNP200     08C74665chr2:
96953275-96953275
AGexonicDe novononsynonymous SNVNM_014014c.T3386Cp.L1129P24.6-Satterstrom2020 E
SNRNP200     AU3777302chr2:
96951536-96951536
TGintronicDe novo--Yuen2017 G
SNRNP200     JASD_Fam0241chr2:
96944354-96944354
CTexonicDe novononsynonymous SNVNM_014014c.G5419Ap.E1807K29.1-Takata2018 E
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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