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Results for "MCM3AP"

Variant Events: 4

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
MCM3AP     iHART2991chr21:
47674759-47674759
CAsplicingPaternalsplicing10.331.657E-5Ruzzo2019 G
MCM3AP     DEASD_0270_001chr21:
47690513-47690514
TATintronicDe novo--Kosmicki2017 E
Satterstrom2020 E
MCM3AP     7-0222-003chr21:
47671485-47671485
GAexonicDe novosynonymous SNVNM_003906c.C4248Tp.S1416S--Yuen2017 G
MCM3AP     72-1921chr21:
47666565-47666565
GAexonicInheritednonsynonymous SNVNM_003906c.C4526Tp.A1509V6.381.657E-5Patowary2019 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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