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Results for "XRCC5"

Variant Events: 10

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
XRCC5     11080.p1chr2:
217001915-217001915
CTexonicDe novosynonymous SNVNM_021141c.C1218Tp.G406G-3.298E-5Krumm2015 E
XRCC5     1-0173-004chr2:
217014945-217014945
AGintronicDe novo--Yuen2017 G
XRCC5     AU030104chr2:
217006268-217006268
TCintronicDe novo--Yuen2017 G
XRCC5     AU3190305chr2:
217066163-217066163
ATintronicDe novo--Yuen2017 G
XRCC5     21.s1chr2:
217024745-217024745
GAintronicDe novo--An2014 E
XRCC5     1-0413-003chr2:
217078634-217078634
ACintergenicDe novo--Yuen2016 G
Yuen2017 G
XRCC5     AU1860302chr2:
217025401-217025401
ATintronicDe novo--Yuen2017 G
XRCC5     2-1266-003chr2:
216980201-216980201
GAintronicDe novo--Yuen2017 G
XRCC5     G01-GEA-267-HIchr2:
216981465-216981465
GCexonicDe novononsynonymous SNVNM_021141c.G219Cp.Q73H22.0-Satterstrom2020 E
XRCC5     14450.p1chr2:
217055072-217055072
GAintronicMosaic, De novo--Dou2017 E
Iossifov2014 E
Kosmicki2017 E
Satterstrom2020 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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