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Results for "SRPRA"
Variant Events: 9
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
SRPRA
7-0356-003
chr11:
126134281-126134281
A
G
exonic
De novo
nonsynonymous SNV
NM_001177842
NM_003139
c.T1595C
c.T1679C
p.V532A
p.V560A
21.2
-
Trost2022
G
Zhou2022
G
E
SRPRA
SP0090669
chr11:
126134377-126134377
T
C
exonic
De novo
nonsynonymous SNV
NM_001177842
NM_003139
c.A1499G
c.A1583G
p.N500S
p.N528S
21.3
8.241E-6
Trost2022
G
SRPRA
4176_18au
chr11:
126138744-126138750
CCGCGTT
C
UTR5
De novo
-
-
Fu2022
E
SRPRA
4B858
chr11:
126135860-126135860
A
ATG
exonic
De novo
frameshift insertion
NM_001177842
NM_003139
c.964_965insCA
c.1048_1049insCA
p.I322fs
p.I350fs
-
-
Fu2022
E
Satterstrom2020
E
Trost2022
G
Zhou2022
G
E
SRPRA
142444
chr11:
126134932-126134933
CA
C
exonic
De novo
frameshift deletion
NM_001177842
NM_003139
c.1362delT
c.1446delT
p.G454fs
p.G482fs
-
-
Fu2022
E
Satterstrom2020
E
Trost2022
G
Zhou2022
G
E
SRPRA
12086.p1
chr11:
126134982-126134982
C
T
exonic
De novo
nonsynonymous SNV
NM_001177842
NM_003139
c.G1313A
c.G1397A
p.R438H
p.R466H
35.0
8.253E-6
Iossifov2014
E
Ji2016
E
Kosmicki2017
E
Krupp2017
E
O’Roak2012b
E
Satterstrom2020
E
Trost2022
G
Turner2017
G
Wilfert2021
G
Zhou2022
G
E
SRPRA
5915
chr11:
126134982-126134982
C
T
exonic
De novo
nonsynonymous SNV
NM_001177842
NM_003139
c.G1313A
c.G1397A
p.R438H
p.R466H
35.0
8.253E-6
Fu2022
E
SRPRA
SP0098898
chr11:
126136699-126136699
C
T
exonic
De novo
synonymous SNV
NM_001177842
NM_003139
c.G561A
c.G645A
p.E187E
p.E215E
-
-
Fu2022
E
Trost2022
G
Zhou2022
G
E
SRPRA
G01-GEA-278-HI
chr11:
126137576-126137576
T
C
exonic
De novo
nonsynonymous SNV
NM_001177842
NM_003139
c.A149G
c.A233G
p.Y50C
p.Y78C
14.57
-
Fu2022
E
Satterstrom2020
E
Trost2022
G
Zhou2022
G
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 notes
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