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Results for "SLC15A1"
Variant Events: 13
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
SLC15A1
152-HSC0079
chr13:
99361005-99361005
C
G
exonic
Inherited
nonsynonymous SNV
NM_005073
c.G1084C
p.A362P
14.11
1.0E-4
Patowary2019
E
SLC15A1
AU2000304
chr13:
99426496-99426496
C
T
intergenic
De novo
-
-
Yuen2017
G
SLC15A1
11940.p1
chr13:
99379122-99379146
AAAACAGAATCCCAATATTAAAGTC
A
intronic
De novo
-
2.0E-4
Satterstrom2020
E
SLC15A1
iHART1908
chr13:
99358483-99358483
C
A
exonic
Maternal
stopgain
NM_005073
c.G1174T
p.G392X
23.0
-
Ruzzo2019
G
SLC15A1
AU024105
chr13:
99369102-99369102
C
T
intronic
De novo
-
-
Yuen2017
G
SLC15A1
12693.p1
chr13:
99360954-99360954
G
T
exonic
Mosaic
nonsynonymous SNV
NM_005073
c.C1135A
p.Q379K
20.7
-
Dou2017
E
SLC15A1
SP0009287
chr13:
99354735-99354735
T
C
exonic
De novo
nonsynonymous SNV
NM_005073
c.A1465G
p.R489G
11.71
-
Feliciano2019
E
Fu2022
E
SLC15A1
SP0057792
chr13:
99368120-99368120
T
G
intronic
De novo
-
-
Fu2022
E
SLC15A1
SP0027031
chr13:
99360880-99360880
T
A
intronic
De novo
-
-
Fu2022
E
SLC15A1
AU4028302
chr13:
99381763-99381763
A
G
intronic
De novo
-
-
Yuen2017
G
SLC15A1
AU0786305
chr13:
99390980-99390980
C
T
intronic
De novo
-
-
Yuen2017
G
SLC15A1
1-0906-003
chr13:
99346119-99346129
GAGTCACACAA
GA
intronic
De novo
-
-
Yuen2017
G
SLC15A1
1-0526-003
chr13:
99429012-99429012
A
AG
intergenic
De 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 notes
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