or
or
Exact

Results for "FLNA"

Variant Events: 5

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
FLNA     JASD_Fam0213chrX:
153580387-153580387
CTexonicDe novononsynonymous SNVNM_001456
NM_001110556
c.G6748A
c.G6772A
p.E2250K
p.E2258K
16.3-Takata2018 E
FLNA     AU4239301chrX:
153601059-153601059
GCintronicDe novo--Yuen2017 G
FLNA     Al-Mubarak2017:ASD-73chrX:
153579330-153579330
AGexonicUnknownnonsynonymous SNVNM_001456
NM_001110556
c.T7079C
c.T7103C
p.V2360A
p.V2368A
22.3-Al-Mubarak2017 E
FLNA     09C86954chrX:
153586885-153586885
ACexonicDe novononsynonymous SNVNM_001110556
NM_001456
c.T4526G
c.T4526G
p.V1509G
p.V1509G
22.7-Satterstrom2020 E
FLNA     Li2017:23663chrX:
153594754-153594754
CTexonicUnknownnonsynonymous SNVNM_001110556
NM_001456
c.G1150A
c.G1150A
p.V384M
p.V384M
12.12-Li2017 T
Source Variant Information

, -

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
More