or
or
Exact

Results for "DPH6"

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
DPH6     2-1336-004chr15:
35708135-35708135
TCintronicDe novo--Yuen2017 G
DPH6     1-0559-004chr15:
35749778-35749778
TCintronicDe novo--Yuen2017 G
DPH6     1-0372-003chr15:
35707449-35707466
CTGTGTGTGTGTGTGTGTCTGTGTGTGTGTGTGTintronicDe novo--Yuen2017 G
DPH6     2-0007-004chr15:
35736443-35736443
TCintronicDe novo--Yuen2017 G
DPH6     AU018Achr15:
35742921-35742921
TCexonicDe novononsynonymous SNVNM_080650c.A470Gp.N157S11.42-DeRubeis2014 E
Kosmicki2017 E
Satterstrom2020 E
DPH6     3-0446-000chr15:
35676747-35676747
CTintronicDe novo--Yuen2016 G
Yuen2017 G
DPH6     iHART3167chr15:
35746972-35746976
TAGTCTexonicPaternalframeshift deletionNM_080650c.358_361delp.D120fs-4.146E-5Ruzzo2019 G
DPH6     AU076509chr15:
35704753-35704753
AGintronicDe novo--Yuen2017 G
DPH6     iHART3168chr15:
35746972-35746976
TAGTCTexonicPaternalframeshift deletionNM_080650c.358_361delp.D120fs-4.146E-5Ruzzo2019 G
Source Variant Information

, -

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
More