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Results for "FCRL6"

Variant Events: 8

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
FCRL6     PN400457chr1:
159779392-159779392
CTexonicUnknownstopgainNM_001004310
NM_001284217
c.C805T
c.C826T
p.Q269X
p.Q276X
10.713.0E-4Leblond2019 E
FCRL6     PN400412chr1:
159779392-159779392
CTexonicUnknownstopgainNM_001004310
NM_001284217
c.C805T
c.C826T
p.Q269X
p.Q276X
10.713.0E-4Leblond2019 E
FCRL6     11524.p1chr1:
159778750-159778750
GAsplicingDe novosplicing11.07-Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Sanders2012 E
Satterstrom2020 E
Willsey2013 E
FCRL6     PN400480chr1:
159779392-159779392
CTexonicUnknownstopgainNM_001004310
NM_001284217
c.C805T
c.C826T
p.Q269X
p.Q276X
10.713.0E-4Leblond2019 E
FCRL6     AU4273304chr1:
159781247-159781247
TGintronicDe novo--Yuen2017 G
FCRL6     SSC00558chr1:
159778750-159778750
GAsplicingDe novosplicing11.07-Lim2017 E
FCRL6     PN400523chr1:
159779392-159779392
CTexonicUnknownstopgainNM_001004310
NM_001284217
c.C805T
c.C826T
p.Q269X
p.Q276X
10.713.0E-4Leblond2019 E
FCRL6     PN400301chr1:
159779392-159779392
CTexonicUnknownstopgainNM_001004310
NM_001284217
c.C805T
c.C826T
p.Q269X
p.Q276X
10.713.0E-4Leblond2019 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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