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Results for "ENTPD1-AS1"

Variant Events: 33

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
ENTPD1-AS1     REACH000349chr10:
97804272-97804272
CGncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     REACH000222 Complex Event; expand row to view variants  De novo--Trost2022 G
Trost2022 G
ENTPD1-AS1     5-0091-003chr10:
97771754-97771754
TCncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     14-1014chr10:
97792704-97792704
CTncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     SP0088384chr10:
97759974-97759974
CAncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     74-0688chr10:
97622263-97622263
TCncRNA_intronicDe novo--Michaelson2012 G
ENTPD1-AS1     2-0149-003chr10:
97641890-97641890
TGncRNA_intronicDe novo--Yuen2017 G
ENTPD1-AS1     2-1325-003chr10:
97756427-97756427
CGncRNA_intronicDe novo--Yuen2016 G
Yuen2017 G
ENTPD1-AS1     4-0064-004chr10:
97770438-97770438
GCncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     2-1402-003chr10:
97725439-97725439
GAncRNA_intronicDe novo--Trost2022 G
Yuen2017 G
ENTPD1-AS1     1-0286-004chr10:
97558890-97558900
CAATATCAGCTCncRNA_intronicDe novo--Trost2022 G
Yuen2017 G
ENTPD1-AS1     2-0307-004chr10:
97743721-97743722
CACncRNA_intronicDe novo--Trost2022 G
Yuen2017 G
ENTPD1-AS1     7-0256-003chr10:
97794144-97794144
CTncRNA_intronicDe novo--Yuen2017 G
ENTPD1-AS1     1-0052-003chr10:
97599662-97599662
GAncRNA_intronicDe novo--Trost2022 G
Yuen2017 G
ENTPD1-AS1     1-0756-003chr10:
97668524-97668524
TAncRNA_intronicDe novo--Yuen2017 G
ENTPD1-AS1     1-0381-003chr10:
97542777-97542807
GGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGGTGTGTGTGTGTTTGTGTGTGTGTGTGTncRNA_intronicDe novo--Yuen2017 G
ENTPD1-AS1     SP0032271chr10:
97604149-97604149
AGncRNA_intronicDe novo--Fu2022 E
ENTPD1-AS1     MSSNG00003-003chr10:
97578868-97578868
AGncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     5-5015-003chr10:
97591086-97591086
AGncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     5-0086-003chr10:
97546007-97546007
GAncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     MSSNG00127-004chr10:
97574099-97574099
GCncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     5-5071-003chr10:
97526381-97526381
CTncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     3-0328-000chr10:
97529348-97529348
GCncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     2-1766-003chr10:
97515958-97515958
AGncRNA_exonicDe novo-2.058E-5Trost2022 G
ENTPD1-AS1     1-0928-003chr10:
97732334-97732334
GCncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     4-0062-003chr10:
97745321-97745322
GGATncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     1-0329-004chr10:
97668539-97668542
TACTGCCGGGCGCGGncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     1-1217-003chr10:
97715919-97715919
ACncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     SP0047210chr10:
97629836-97629836
TCncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     3-0198-000chr10:
97668539-97668542
TACTGCCGGGCGCncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     13515.p1chr10:
97657174-97657174
CTncRNA_intronicDe novo--Turner2016 G
ENTPD1-AS1     4-0056-003chr10:
97619327-97619327
CTncRNA_intronicDe novo--Trost2022 G
ENTPD1-AS1     MSSNG00158-003chr10:
97627107-97627107
ATncRNA_intronicDe novo--Trost2022 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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