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Results for "FAM76B"

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
FAM76B     MSSNG00436-003chr11:
95521730-95521730
GCintronicDe novo--Trost2022 G
Zhou2022 GE
FAM76B     2-1336-003chr11:
95516280-95516280
TCexonicDe novononsynonymous SNVNM_144664c.A512Gp.H171R13.22-Yuen2015 G
Yuen2017 G
Zhou2022 GE
FAM76B     2-1477-003chr11:
95501714-95501714
CGdownstreamDe novo--Trost2022 G
Yuen2016 G
Yuen2017 G
FAM76B     1-0901-003chr11:
95520121-95520122
TCATintronicDe novo--Trost2022 G
FAM76B     SP0224004chr11:
95511959-95511959
CTintronicDe novo--Trost2022 G
FAM76B     AU1933302chr11:
95503985-95503985
ACUTR3De novo--Yuen2017 G
FAM76B     mAGRE5191chr11:
95522621-95522621
CGexonicDe novononsynonymous SNVNM_144664c.G22Cp.A8P31.0-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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