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Results for "LRRK2"

Variant Events: 32

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
LRRK2     A09018-3chr12:
40702952-40702952
CTexonicUnknownstopgainNM_198578c.C4234Tp.R1412X44.0-Li2017 T
LRRK2     MSSNG00251-003chr12:
40742702-40742702
GAintronicDe novo--Trost2022 G
LRRK2     mAGRE2748chr12:
40753248-40753248
TCsplicingPaternalsplicing17.071.658E-5Cirnigliaro2023 G
LRRK2     A7chr12:
40702952-40702952
CTexonicDe novostopgainNM_198578c.C4234Tp.R1412X44.0-Wu2018 G
LRRK2     Li2017:23636chr12:
40702346-40702346
GAexonicUnknownnonsynonymous SNVNM_198578c.G4037Ap.G1346D28.1-Li2017 T
LRRK2     AU2463301chr12:
40696892-40696892
GAintronicDe novo--Trost2022 G
LRRK2     10-0001-003chr12:
40730879-40730879
CGintronicDe novo--Trost2022 G
LRRK2     AU038204chr12:
40687350-40687350
GTexonicDe novononsynonymous SNVNM_198578c.G2693Tp.S898I15.31-Trost2022 G
Yuen2017 G
Zhou2022 GE
LRRK2     AU3399302chr12:
40766507-40766507
GTintergenicDe novo--Yuen2017 G
LRRK2     1-0563-003chr12:
40721453-40721453
GAintronicDe novo--Trost2022 G
Yuen2017 G
LRRK2     2-1213-003chr12:
40779224-40779224
GTintergenicDe novo--Yuen2017 G
LRRK2     AU070703chr12:
40715947-40715947
AGexonicDe novononsynonymous SNVNM_198578c.A5281Gp.S1761G21.5-Trost2022 G
Yuen2017 G
Zhou2022 GE
LRRK2     iHART2748chr12:
40753248-40753248
TCsplicingPaternalsplicing17.071.658E-5Ruzzo2019 G
LRRK2     AU2156303chr12:
40676145-40676145
GAintronicDe novo--Trost2022 G
Yuen2017 G
LRRK2     2-1811-004chr12:
40629287-40629287
GTintronicDe novo--Trost2022 G
LRRK2     7-0457-004chr12:
40636066-40636066
TAintronicDe novo--Trost2022 G
LRRK2     Li2017:19687chr12:
40715839-40715839
CTexonicUnknownstopgainNM_198578c.C5173Tp.R1725X45.06.637E-5Li2017 T
LRRK2     SP0019599chr12:
40707817-40707817
AGexonicDe novononsynonymous SNVNM_198578c.A4580Gp.Y1527C23.5-Fu2022 E
Trost2022 G
Zhou2022 GE
LRRK2     1-0647-003chr12:
40624501-40624501
ATintronicDe novo--Trost2022 G
LRRK2     2-1811-004chr12:
40629265-40629265
ACintronicDe novo--Trost2022 G
LRRK2     3-0436-000chr12:
40766587-40766587
CTintergenicDe novo--Yuen2016 G
Yuen2017 G
LRRK2     MSSNG00066-003chr12:
40678903-40678903
CTintronicDe novo--Trost2022 G
LRRK2     SP0225491chr12:
40681330-40681330
TCexonicDe novononsynonymous SNVNM_198578c.T2678Cp.L893P13.92-Trost2022 G
LRRK2     MSSNG00002-004chr12:
40657812-40657812
TAintronicDe novo--Trost2022 G
LRRK2     2-0102-004chr12:
40668397-40668397
CTexonicDe novononsynonymous SNVNM_198578c.C1669Tp.P557S23.1-Trost2022 G
Yuen2015 G
Zhou2022 GE
LRRK2     1-0186-005chr12:
40673006-40673009
GTTTCGCGCCCGintronicDe novo--Trost2022 G
LRRK2     1-0242-003chr12:
40654631-40654631
TCintronicDe novo--Trost2022 G
LRRK2     Li2017:19764chr12:
40704416-40704416
CTexonicUnknownnonsynonymous SNVNM_198578c.C4501Tp.R1501W25.38.276E-6Li2017 T
LRRK2     SP0005499chr12:
40629502-40629502
TGexonicDe novononsynonymous SNVNM_198578c.T422Gp.L141R17.257.441E-5Fu2022 E
Zhou2022 GE
LRRK2     MSSNG00088-003chr12:
40654656-40654656
AGintronicDe novo--Trost2022 G
LRRK2     1-1184-003chr12:
40644246-40644246
TAintronicDe novo--Trost2022 G
LRRK2     1-1040-004chr12:
40651113-40651113
AGexonicDe novononsynonymous SNVNM_198578c.A1352Gp.K451R11.85-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 notesView
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