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Results for "RFT1"

Variant Events: 9

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
RFT1     MT_69chr3:
53156434-53156434
GTexonicMaternalnonsynonymous SNVNM_052859c.C412Ap.P138T20.9-Toma2013 E
RFT1     AU3052303chr3:
53144904-53144904
CTintronicDe novo--Yuen2017 G
RFT1     2-0210-004chr3:
53175455-53175455
GAintergenicDe novo--Yuen2017 G
RFT1     2-1702-003chr3:
53135460-53135460
GCintronicDe novo--Yuen2017 G
RFT1     AU4336301chr3:
53137627-53137627
CTintronicDe novo--Yuen2017 G
RFT1     1-0321-004chr3:
53191681-53191681
AGintergenicDe novo--Yuen2017 G
RFT1     AU009805chr3:
53173380-53173380
CGintergenicDe novo--Yuen2017 G
RFT1     1-0043-004chr3:
53147353-53147353
GCintronicDe novo--Yuen2017 G
RFT1     SP0081957chr3:
53133520-53133520
ACintronicDe novo--Fu2022 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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