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Results for "CACNA1S"
Variant Events: 22
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
CACNA1S
Viggiano2022:14.4
chr1:
201044667-201044667
A
G
exonic
Paternal
nonsynonymous SNV
NM_000069
c.T1904C
p.M635T
15.14
4.118E-5
Viggiano2022
G
T
CACNA1S
Viggiano2022:49.3
chr1:
201031603-201031603
C
G
exonic
Maternal
nonsynonymous SNV
NM_000069
c.G2893C
p.E965Q
15.52
8.238E-6
Viggiano2022
G
T
CACNA1S
12916.p1
chr1:
201061169-201061169
C
T
exonic
De novo
nonsynonymous SNV
NM_000069
c.G472A
p.G158S
28.4
8.238E-6
Iossifov2012
E
Iossifov2014
E
Ji2016
E
Kosmicki2017
E
Krupp2017
E
Satterstrom2020
E
Zhou2022
G
E
CACNA1S
1-0433-003
chr1:
201069206-201069206
C
T
intronic
De novo
-
-
Trost2022
G
Yuen2017
G
CACNA1S
SSC05167
chr1:
201047218-201047218
C
T
exonic
De novo
nonsynonymous SNV
NM_000069
c.G1408A
p.V470M
15.31
-
Fu2022
E
Lim2017
E
Trost2022
G
CACNA1S
SSC06435
chr1:
201061169-201061169
C
T
exonic
De novo
nonsynonymous SNV
NM_000069
c.G472A
p.G158S
28.4
8.238E-6
Fu2022
E
Trost2022
G
CACNA1S
14292.p1
chr1:
201009260-201009260
T
G
intronic
De novo
-
8.334E-6
Satterstrom2020
E
CACNA1S
12472.p1
chr1:
201047218-201047218
C
T
exonic
De novo
nonsynonymous SNV
NM_000069
c.G1408A
p.V470M
15.31
-
Iossifov2014
E
Ji2016
E
Kosmicki2017
E
Krupp2017
E
Satterstrom2020
E
Wilfert2021
G
Zhou2022
G
E
CACNA1S
Viggiano2022:46.3
chr1:
201020224-201020224
T
C
exonic
Maternal
nonsynonymous SNV
NM_000069
c.A4001G
p.Y1334C
15.94
1.647E-5
Viggiano2022
G
T
CACNA1S
Viggiano2022:40.4
chr1:
201017745-201017747
GCA
G
exonic
Maternal
frameshift deletion
NM_000069
c.4404_4405del
p.F1468fs
-
-
Viggiano2022
G
T
CACNA1S
iHART3273
chr1:
201054636-201054640
CTAGT
C
exonic
Maternal
frameshift deletion
NM_000069
c.1074_1077del
p.Q358fs
-
-
Ruzzo2019
G
CACNA1S
iHART1048
chr1:
201052451-201052451
C
T
splicing
Maternal
splicing
14.2
8.237E-6
Ruzzo2019
G
CACNA1S
9190768
chr1:
201010738-201010738
G
T
intronic
De novo
-
-
Fu2022
E
CACNA1S
AU4056302
chr1:
201054636-201054640
CTAGT
C
exonic
Maternal
frameshift deletion
NM_000069
c.1074_1077del
p.Q358fs
-
-
Cirnigliaro2023
G
CACNA1S
mAGRE1048
chr1:
201052451-201052451
C
T
splicing
Maternal
splicing
14.2
8.237E-6
Cirnigliaro2023
G
CACNA1S
NDAR_INVAF559YZC_wes1
chr1:
201009483-201009483
G
C
exonic
De novo
nonsynonymous SNV
NM_000069
c.C5246G
p.S1749C
6.996
-
DeRubeis2014
E
Fu2022
E
Kosmicki2017
E
Lim2017
E
Satterstrom2020
E
Trost2022
G
Zhou2022
G
E
CACNA1S
13999.p1
chr1:
201063110-201063110
C
T
exonic
Mosaic
nonsynonymous SNV
NM_000069
c.G298A
p.E100K
32.0
-
Dou2017
E
CACNA1S
302-05-103645
chr1:
201022412-201022412
G
A
intronic
De novo
-
4.13E-5
Satterstrom2020
E
Trost2022
G
CACNA1S
111300
chr1:
201046190-201046190
A
T
exonic
nonsynonymous SNV
NM_000069
c.T1685A
p.L562Q
23.9
-
Woodbury-Smith2022
E
CACNA1S
SP0065412
chr1:
201047106-201047106
C
T
exonic
nonsynonymous SNV
NM_000069
c.G1520A
p.G507D
31.0
-
Zhou2022
G
E
CACNA1S
SP0036774
chr1:
201020199-201020199
C
T
exonic
synonymous SNV
NM_000069
c.G4026A
p.S1342S
-
8.237E-6
Zhou2022
G
E
CACNA1S
6584
chr1:
201009260-201009260
T
G
intronic
De novo
-
8.334E-6
Trost2022
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 notes
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