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Results for "MLLT10"

Variant Events: 14

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
MLLT10     1-0935-003chr10:
21916946-21916946
CGintronicDe novo--Yuen2017 G
MLLT10     AU045514chr10:
21945419-21945419
GAintronicDe novo--Yuen2017 G
MLLT10     2-1338-003chr10:
21839736-21839736
CGintronicDe novo--Yuen2017 G
MLLT10     AU015903chr10:
21932182-21932182
GAintronicDe novo--Yuen2017 G
MLLT10     A1chr10:
21952954-21952954
TCintronicDe novo--Wu2018 G
MLLT10     2-0278-003chr10:
21909237-21909237
CTintronicDe novo--Yuen2017 G
MLLT10     2-1382-003chr10:
22000788-22000788
TCintronicDe novo--Yuen2016 G
MLLT10     13951.p1chr10:
21986318-21986318
CTintronicDe novo--Turner2016 G
MLLT10     1-0226-005chr10:
21967182-21967182
CTintronicDe novo--Yuen2017 G
MLLT10     AU071804chr10:
21866834-21866841
ATTTTTTTATTTTTTintronicDe novo--Yuen2017 G
MLLT10     15.s1chr10:
21962536-21962536
CGexonicDe novononsynonymous SNVNM_001195626
NM_004641
c.C1309G
c.C1309G
p.P437A
p.P437A
14.59-An2014 E
MLLT10     AU4412302chr10:
22020804-22020804
TGintronicDe novo--Yuen2017 G
MLLT10     5-0088-003chr10:
21857352-21857352
AGintronicDe novo--Yuen2017 G
MLLT10     2-0310-003chr10:
22042744-22042744
GCintergenicDe novo--Yuen2017 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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