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Results for "PARP6"

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
PARP6     1-0024-003chr15:
72543821-72543821
TCintronicDe novo--Yuen2016 G
Yuen2017 G
PARP6     2-1373-003chr15:
72538187-72538187
GCintronicDe novo--Yuen2017 G
PARP6     2-0297-003chr15:
72565146-72565146
GTintergenicDe novo--Yuen2017 G
PARP6     iHART3004chr15:
72542407-72542408
GAGexonicMaternalframeshift deletionNM_020214c.1444delTp.S482fs--Ruzzo2019 G
PARP6     iHART3007chr15:
72542407-72542408
GAGexonicMaternalframeshift deletionNM_020214c.1444delTp.S482fs--Ruzzo2019 G
PARP6     13038.p1 Complex Event; expand row to view variants  De novo--Dong2014 E
Iossifov2012 E
Iossifov2014 E
Kosmicki2017 E
Satterstrom2020 E
Wilfert2021 G
PARP6     AU4013303chr15:
72565757-72565757
GCintergenicDe 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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