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Results for "SORD"

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
SORD     12610.p1chr15:
45365730-45365730
GAUTR3De novo-0.034Iossifov2014 E
Kosmicki2017 E
SORD     1-0353-003chr15:
45321407-45321407
TAintronicDe novo--Yuen2017 G
SORD     200675733@1082034734chr15:
45353297-45353297
CTexonicDe novostopgainNM_003104c.C298Tp.R100X19.098.239E-6Satterstrom2020 E
SORD     AU3398301chr15:
45325619-45325619
GAintronicDe novo--Yuen2017 G
SORD     60-1015chr15:
45335545-45335545
AGexonicInheritednonsynonymous SNVNM_003104c.A191Gp.K64R13.433.0E-4Patowary2019 E
SORD     1-0674-004chr15:
45356642-45356642
GAintronicDe novo--Yuen2017 G
SORD     AU3907302chr15:
45339235-45339238
CAAACAAintronicDe novo--Yuen2017 G
SORD     Chen2017:119chr15:
45353297-45353297
CTexonicDe novostopgainNM_003104c.C298Tp.R100X19.098.239E-6Chen2017 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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