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Results for "HSPG2"

Variant Events: 43

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
HSPG2     2-1451-003chr1:
22181309-22181309
TCintronicDe novo--Yuen2017 G
HSPG2     2-0244-004chr1:
22259478-22259478
GAintronicDe novo--Trost2022 G
Yuen2017 G
HSPG2     MT_160.4chr1:
22194106-22194106
CTintronicDe novo--Trost2022 G
HSPG2     12385.p1chr1:
22181274-22181279
GGGTCAGintronicDe novo--Iossifov2014 E
Kosmicki2017 E
Satterstrom2020 E
HSPG2     68695chr1:
22181274-22181279
GGGTCAGintronicDe novo--Trost2022 G
HSPG2     SP0119755chr1:
22217179-22217179
GAexonicDe novostopgainNM_001291860
NM_005529
c.C253T
c.C253T
p.R85X
p.R85X
24.78.273E-6Fu2022 E
Trost2022 G
Zhou2022 GE
HSPG2     REACH000697chr1:
22219593-22219593
GAintronicDe novo--Trost2022 G
HSPG2     MSSNG00041-004chr1:
22200384-22200384
CAintronicDe novo--Trost2022 G
HSPG2     SP0082859chr1:
22161367-22161367
CTexonicDe novononsynonymous SNVNM_001291860
NM_005529
c.G10528A
c.G10525A
p.E3510K
p.E3509K
17.852.0E-4Trost2022 G
Zhou2022 GE
HSPG2     1-0483-004chr1:
22168256-22168256
CAintronicDe novo--Trost2022 G
HSPG2     MSSNG00353-004chr1:
22153807-22153807
CTintronicDe novo--Trost2022 G
HSPG2     SP0036988chr1:
22172777-22172778
AGAintronicDe novo--Fu2022 E
Trost2022 G
HSPG2     SP0114190chr1:
22155617-22155617
GTintronicDe novo--Fu2022 E
Trost2022 G
HSPG2     SP0139290chr1:
22175274-22175274
CAexonicDe novosynonymous SNVNM_001291860
NM_005529
c.G7602T
c.G7599T
p.A2534A
p.A2533A
--Fu2022 E
Trost2022 G
Zhou2022 GE
HSPG2     SP0046238chr1:
22206783-22206783
CTintronicDe novo-2.0E-4Fu2022 E
Trost2022 G
HSPG2     SP0008211chr1:
22186217-22186217
CTintronicDe novo--Fu2022 E
HSPG2     SP0128722chr1:
22214482-22214482
GAexonicDe novononsynonymous SNVNM_001291860
NM_005529
c.C652T
c.C652T
p.R218C
p.R218C
25.41.65E-5Fu2022 E
Trost2022 G
Zhou2022 GE
HSPG2     2-1519-006chr1:
22224098-22224098
GAintronicDe novo--Trost2022 G
HSPG2     AU1448301chr1:
22268235-22268237
CCCCCCTGTGACCAATTATATCCCCTGTGACCintergenicDe novo--Yuen2017 G
HSPG2     SP0125472chr1:
22180817-22180817
CTexonicDe novononsynonymous SNVNM_001291860
NM_005529
c.G6311A
c.G6308A
p.R2104Q
p.R2103Q
24.41.0E-4Fu2022 E
Trost2022 G
Zhou2022 GE
HSPG2     REACH000714chr1:
22223505-22223505
CGintronicDe novo--Trost2022 G
HSPG2     SP0052719chr1:
22160354-22160354
GAexonicDe novosynonymous SNVNM_001291860
NM_005529
c.C10788T
c.C10785T
p.P3596P
p.P3595P
--Fu2022 E
Trost2022 G
Zhou2022 GE
HSPG2     SP0014140chr1:
22207303-22207303
CTexonicDe novononsynonymous SNVNM_001291860
NM_005529
c.G1847A
c.G1844A
p.R616H
p.R615H
12.913.0E-4Fu2022 E
Trost2022 G
Zhou2022 GE
HSPG2     AU059003chr1:
22249451-22249451
CTintronicDe novo--Trost2022 G
HSPG2     SSC00193chr1:
22199230-22199230
GTexonicDe novostopgainNM_001291860
NM_005529
c.C3915A
c.C3912A
p.C1305X
p.C1304X
42.0-Fu2022 E
Lim2017 E
HSPG2     12763.p1chr1:
22263991-22263991
CGupstreamDe novo--Wilfert2021 G
HSPG2     11089.p1chr1:
22162442-22162442
AGintronicDe novo--Turner2016 G
HSPG2     mAGRE3119chr1:
22178283-22178283
CTsplicingPaternalsplicing22.2-Cirnigliaro2023 G
HSPG2     mAGRE2382chr1:
22149892-22149892
GAexonicPaternalstopgainNM_001291860
NM_005529
c.C13096T
c.C13093T
p.R4366X
p.R4365X
53.01.0E-4Cirnigliaro2023 G
HSPG2     NDAR_INVWK012EYC_wes1chr1:
22174444-22174444
CTintronicDe novo8.56-DeRubeis2014 E
Fu2022 E
Kosmicki2017 E
Lim2017 E
Satterstrom2020 E
Trost2022 G
Zhou2022 GE
HSPG2     36097chr1:
22172681-22172681
ACexonicDe novononsynonymous SNVNM_001291860
NM_005529
c.T8387G
c.T8384G
p.V2796G
p.V2795G
13.36-Fu2022 E
HSPG2     4771021312387-Cchr1:
22207174-22207174
TCexonicDe novononsynonymous SNVNM_001291860
NM_005529
c.A1976G
c.A1973G
p.N659S
p.N658S
20.8-Fu2022 E
HSPG2     11442.p1chr1:
22199230-22199230
GTexonicDe novostopgainNM_001291860
NM_005529
c.C3915A
c.C3912A
p.C1305X
p.C1304X
42.0-Ji2016 E
Krumm2015 E
Zhou2022 GE
HSPG2     F10267-1chr1:
22215188-22215188
CGintronicDe novo--Fu2022 E
Satterstrom2020 E
Trost2022 G
HSPG2     mAGRE2873chr1:
22207221-22207221
GCexonicMaternalstopgainNM_001291860
NM_005529
c.C1929G
c.C1926G
p.Y643X
p.Y642X
22.1-Cirnigliaro2023 G
HSPG2     mAGRE2872chr1:
22207221-22207221
GCexonicMaternalstopgainNM_001291860
NM_005529
c.C1929G
c.C1926G
p.Y643X
p.Y642X
22.1-Cirnigliaro2023 G
HSPG2     mAGRE3115chr1:
22202171-22202171
CAexonicDe novononsynonymous SNVNM_001291860
NM_005529
c.G3256T
c.G3253T
p.D1086Y
p.D1085Y
11.12-Cirnigliaro2023 G
HSPG2     iHART2872chr1:
22207221-22207221
GCexonicMaternalstopgainNM_001291860
NM_005529
c.C1929G
c.C1926G
p.Y643X
p.Y642X
22.1-Ruzzo2019 G
HSPG2     AU1725302chr1:
22163866-22163866
CGintronicDe novo--Trost2022 G
Yuen2017 G
HSPG2     AU1860302chr1:
22275220-22275220
CTintergenicDe novo--Yuen2017 G
HSPG2     iHART3119chr1:
22178283-22178283
CTsplicingPaternalsplicing22.2-Ruzzo2019 G
HSPG2     iHART2873chr1:
22207221-22207221
GCexonicMaternalstopgainNM_001291860
NM_005529
c.C1929G
c.C1926G
p.Y643X
p.Y642X
22.1-Ruzzo2019 G
HSPG2     iHART3115chr1:
22202171-22202171
CAexonicDe novononsynonymous SNVNM_001291860
NM_005529
c.G3256T
c.G3253T
p.D1086Y
p.D1085Y
11.12-Ruzzo2019 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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