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Results for "FAM110B"

Variant Events: 14

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
FAM110B     AU2433303chr8:
59125641-59125641
AGintergenicDe novo--Yuen2017 G
FAM110B     AU3794301chr8:
59132648-59132648
TCintergenicDe novo--Yuen2017 G
FAM110B     1-0433-004chr8:
59032766-59032766
GAintronicDe novo--Yuen2017 G
FAM110B     AU1988302chr8:
59077277-59077277
CTintergenicDe novo--Yuen2017 G
FAM110B     AU1725306chr8:
59100339-59100339
AGintergenicDe novo--Yuen2017 G
FAM110B     AU4012302chr8:
59103104-59103104
GAintergenicDe novo--Yuen2017 G
FAM110B     7-0179-003chr8:
59152775-59152783
GAAGTAAGTGAAGTintergenicDe novo--Yuen2017 G
FAM110B     AU058105chr8:
59004556-59004556
CTintronicDe novo--Yuen2017 G
FAM110B     11946.p1chr8:
58926192-58926193
TGTintronicDe novo--Werling2018 G
FAM110B     AU3874303chr8:
58930706-58930706
AGintronicDe novo--Yuen2017 G
FAM110B     AU059903chr8:
59118395-59118395
GAintergenicDe novo--Yuen2017 G
FAM110B     2-1290-003chr8:
59138307-59138307
CTintergenicDe novo--Yuen2017 G
FAM110B     7-0148-003chr8:
59014153-59014153
GAintronicDe novo--Yuen2017 G
FAM110B     2-1629-003chr8:
58922883-58922883
GAintronicDe novo--Yuen2017 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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