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Results for "CROCC"

Variant Events: 6

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
CROCC     AU3692301chr1:
17277584-17277584
CTexonicDe novosynonymous SNVNM_014675c.C2973Tp.H991H-4.251E-5Yuen2017 G
CROCC     12325.p1chr1:
17263235-17263235
GAexonicDe novononsynonymous SNVNM_014675c.G1060Ap.E354K0.9564.213E-5Iossifov2014 E
Kosmicki2017 E
CROCC     JASD_Fam0207chr1:
17272061-17272061
TCexonicDe novononsynonymous SNVNM_014675c.T2096Cp.L699P9.942-Takata2018 E
CROCC     1-0986-003chr1:
17284427-17284427
CTintronicDe novo--Yuen2017 G
CROCC     AU2458302chr1:
17258404-17258404
GAintronicDe novo--Yuen2017 G
CROCC     NDAR_INVPC670BF4_wes1chr1:
17250836-17250836
AGexonicDe novosynonymous SNVNM_014675c.A213Gp.T71T-0.3367DeRubeis2014 E
Kosmicki2017 E
Satterstrom2020 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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