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Results for "MCM6"

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
MCM6     3-0456-000chr2:
136644026-136644026
GAintergenicDe novo--Yuen2016 G
Yuen2017 G
MCM6     AU038203chr2:
136617003-136617003
CTexonicDe novosynonymous SNVNM_005915c.G1230Ap.E410E--Yuen2017 G
MCM6     14216.p1chr2:
136610419-136610419
GAexonicDe novononsynonymous SNVNM_005915c.C1693Tp.R565C15.74-Iossifov2014 E
Ji2016 E
Kosmicki2017 E
Satterstrom2020 E
MCM6     3-0456-000Bchr2:
136644026-136644026
GAintergenicDe novo--Yuen2017 G
MCM6     JASD_Fam0186chr2:
136626351-136626351
GAexonicDe novononsynonymous SNVNM_005915c.C445Tp.P149S33.0-Takata2018 E
MCM6     2-1292-003chr2:
136603919-136603919
GAexonicDe novosynonymous SNVNM_005915c.C2097Tp.Y699Y--Yuen2015 G
Yuen2017 G
MCM6     AU3632301chr2:
136623283-136623283
CAintronicDe novo--Yuen2017 G
MCM6     NP140chr2:
136626351-136626351
GAexonicDe novononsynonymous SNVNM_005915c.C445Tp.P149S33.0-Lim2017 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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