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Results for "ZWILCH"

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
ZWILCH     1-0551-003chr15:
66809135-66809135
CTintronicDe novo--Yuen2017 G
ZWILCH     iHART2367chr15:
66832550-66832550
TCsplicingMaternalsplicing13.892.493E-5Ruzzo2019 G
ZWILCH     2-0070-003chr15:
66821214-66821214
GGCexonicDe novoframeshift insertionNM_001287822
NM_001287823
NM_001287821
NM_017975
c.652_653insC
c.652_653insC
c.652_653insC
c.994_995insC
p.V218fs
p.V218fs
p.V218fs
p.V332fs
--Yuen2015 G
ZWILCH     12859.p1 Complex Event; expand row to view variants  De novo-8.259E-6Iossifov2012 E
Iossifov2014 E
Kosmicki2017 E
Satterstrom2020 E
ZWILCH     14175.p1 Complex Event; expand row to view variants  De novostopgain, frameshift insertionNM_001287822
NM_001287823
NM_001287821
NM_017975
NM_001287822
NM_001287823
NM_001287821
NM_017975
NM_001287822
NM_001287823
NM_001287821
NM_017975
c.1364_1365insG
c.1364_1365insG
c.1364_1365insG
c.1706_1707insG
c.1365_1366insG
c.1365_1366insG
c.1365_1366insG
c.1707_1708insG
c.1364_1365insGTAATTCCTGTGTTAACACTG
c.1364_1365insGTAATTCCTGTGTTAACACTG
c.1364_1365insGTAATTCCTGTGTTAACACTG
c.1706_1707insGTAATTCCTGTGTTAACACTG
p.L455fs
p.L455fs
p.L455fs
p.L569fs
p.L455fs
p.L455fs
p.L455fs
p.L569fs
p.L455delinsLX
p.L455delinsLX
p.L455delinsLX
p.L569delinsLX
--Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Satterstrom2020 E
Wilfert2021 G
ZWILCH     iHART2366chr15:
66832550-66832550
TCsplicingMaternalsplicing13.892.493E-5Ruzzo2019 G
ZWILCH     7-0100-003chr15:
66803818-66803818
GAintronicDe novo--Yuen2017 G
ZWILCH     iHART3051chr15:
66820193-66820193
AGsplicingMaternalsplicing17.94-Ruzzo2019 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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