Global Variome shared LOVD
MSH2 (mutS homolog 2, colon cancer, nonpolyposis ty...)
LOVD v.3.0 Build 29 [
Current LOVD status
]
Register as submitter
|
Log in
Curators:
InSiGHT - John-Paul Plazzer
,
Mev Dominguez Valentin
, and
Bryony A Thompson
View all genes
View MSH2 gene homepage
View graphs about the MSH2 gene database
Create a new gene entry
View all transcripts
View all transcripts of gene MSH2
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene MSH2
View all variants in gene MSH2
Full data view for gene MSH2
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
View all individuals with variants in gene MSH2
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene MSH2
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene MSH2
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
All screenings for gene MSH2
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Template
: Template(s) used to detect the sequence variant; DNA (genomic DNA), RNA (cDNA) or protein
All options:
DNA
RNA = RNA (cDNA)
protein
? = unknown
Technique
: technique(s) used to identify the sequence variant.
All options:
? = unknown
ARMS = amplification refractory mutation system
arrayCGH = array for Comparative Genomic Hybridisation
arraySEQ = array for resequencing
arraySNP = array for SNP typing
arrayCNV = array for Copy Number Variation (SNP and CNV probes)
ASO = allele-specific oligo hybridisation
BESS = Base Excision Sequence Scanning
CMC = Chemical Mismatch Cleavage
COBRA = Combined Bisulfite Restriction Analysis
CSCE = Conformation Sensitive Capillary Electrophoresis
CSGE = Conformation Sensitive Gel Electrophoresis
ddF = dideoxy Fingerprinting
DGGE = Denaturing-Gradient Gel-Electrophoresis
DHPLC = Denaturing High-Performance Liquid Chromatography
DOVAM = Detection Of Virtually All Mutations (SSCA variant)
DSCA = Double-Strand DNA Conformation Analysis
DSDI = Detection Small Deletions and Insertions
EMC = Enzymatic Mismatch Cleavage
expr = expression analysis
FISH = Fluorescent In-Situ Hybridisation
FISHf = fiberFISH
HD = HeteroDuplex analysis
HPLC = High-Performance Liquid Chromatography
IEF = IsoElectric Focussing
IHC = Immuno-Histo-Chemistry
Invader = Invader assay
MAPH = Multiplex Amplifiable Probe Hybridisation
MAQ = Multiplex Amplicon Quantification
MCA = Melting Curve Analysis, high-resolution (HRMA)
microscope = microscopic analysis (karyotype)
microsat = microsatellite genotyping
minigene = expression minigene construct
MIP = Molecular Inversion Probe amplification
MIPsm = singele molecule Molecular Inversion Probe amplification
MLPA = Multiplex Ligation-dependent Probe Amplification
MLPA-ms = Multiplex Ligation-dependent Probe Amplification, methylation specific
MS = mass spectrometry
Northern = Northern blotting
NUC = nuclease digestion (RNAseT1, S1)
OM = optical mapping
PAGE = Poly-Acrylamide Gel-Electrophoresis
PCR = Polymerase Chain Reaction
PCRdd = PCR, digital droplet
PCRdig = PCR + restriction enzyme digestion
PCRh = PCR, haloplex
PCRlr = PCR, long-range
PCRm = PCR, multiplex
PCRms = PCR, methylation sensitive
PCRq = PCR, quantitative (qPCR)
PCRrp = PCR, repeat-primed (RP-PCR)
PCRsqd = PCR, semi-quantitative duplex
PE = primer extension (APEX, SNaPshot)
PEms = primer extension, methylation-sensitive single-nucleotide
PFGE = Pulsed-Field Gel-Electrophoresis (+Southern)
PTT = Protein Truncation Test
RFLP = Restriction Fragment Length Polymorphisms
RT-PCR = Reverse Transcription and PCR
RT-PCRq = Reverse Transcription and PCR, quantitative
SBE = Single Base Extension
SEQ = SEQuencing (Sanger)
SEQb = bisulfite SEQuencing
SEQp = pyroSequencing
SEQms = sequencing, methylation specific
SEQ-ON = next-generation sequencing - Oxford Nanopore
SEQ-NG = next-generation sequencing
SEQ-NG-RNA = next-generation sequencing RNA
SEQ-NG-H = next-generation sequencing - Helicos
SEQ-NG-I = next-generation sequencing - Illumina/Solexa
SEQ-NG-IT = next-generation sequencing - Ion Torrent
SEQ-NG-R = next-generation sequencing - Roche/454
SEQ-NG-S = next-generation sequencing - SOLiD
SEQ-PB = next-generation sequencing - Pacific Biosciences
SNPlex = SNPlex
Southern = Southern blotting
SSCA = Single-Strand DNA Conformation polymorphism Analysis (SSCP)
SSCAf = fluorescent SSCA (SSCP)
STR = Short Tandem Repeat
TaqMan = TaqMan assay
Western = Western blotting
- = not applicable
Tissue
: tissue type used for analysis
Remarks
: remarks regarding the screening like WGS (whole genome sequencing), WES (whole exome sequencing, gene panel (incl. a list of genes analysed), etc.
How to query this table
All list views have search fields which can be used to search data. You can search for a complete word or you can search for a part of a search term. If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify. Note that search terms are case-insensitive and that wildcards such as * are treated as normal text! For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.
Operator
Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
Arg Ser
all entries containing 'Arg' and 'Ser'
|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
Text
!=""
all entries with this field not empty
!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
>=
Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
To sort on a certain column, click on the column header or on the arrows. If that column is already selected to sort on, the sort order will be swapped. The column currently sorted on has a darker blue background color than the other columns. The up and down arrows next to the column name indicate the current sorting direction. When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.
7041 entries on 71 pages. Showing entries 1 - 100.
10 per page
25 per page
50 per page
100 per page
250 per page
500 per page
1000 per page
Legend
How to query
« First
Prev
1
2
3
4
5
6
7
8
9
10
11
...
Next
Last »
Screening ID
Individual ID
Template
Technique
Tissue
Remarks
Variants found
Owner
0000003190
00003272
DNA
SEQ-NG-I
-
-
1
Christopher Watson
0000003192
00003274
DNA
SEQ-NG-I
-
-
1
Christopher Watson
0000003196
00003278
DNA
SEQ-NG-I
-
-
1
Christopher Watson
0000003200
00003281
DNA
SEQ-NG-I
-
-
1
Christopher Watson
0000036292
00036222
DNA
SEQ
-
-
1
Andreas Laner
0000036293
00036223
DNA
SEQ
-
-
1
Andreas Laner
0000036294
00036224
DNA
SEQ
-
-
1
Andreas Laner
0000036295
00036225
DNA
SEQ
-
-
1
Andreas Laner
0000036296
00036226
DNA
SEQ
-
-
1
Andreas Laner
0000036297
00036227
DNA
SEQ
-
-
1
Andreas Laner
0000036298
00036228
DNA
SEQ
-
-
1
Andreas Laner
0000036299
00036229
DNA
SEQ
-
-
1
Andreas Laner
0000036300
00036230
DNA
SEQ
-
-
1
Andreas Laner
0000036301
00036231
DNA
SEQ
-
-
1
Andreas Laner
0000036302
00036232
DNA
SEQ
-
-
1
Andreas Laner
0000036303
00036233
DNA
SEQ
-
-
1
Andreas Laner
0000036304
00036234
DNA
SEQ
-
-
1
Andreas Laner
0000036305
00036235
DNA
SEQ
-
-
1
Andreas Laner
0000036306
00036236
DNA
SEQ
-
-
1
Andreas Laner
0000036307
00036237
DNA
SEQ
-
-
1
Andreas Laner
0000036308
00036238
DNA
SEQ
-
-
1
Andreas Laner
0000036309
00036239
DNA
SEQ
-
-
1
Andreas Laner
0000036310
00036240
DNA
SEQ
-
-
1
Andreas Laner
0000036311
00036241
DNA
SEQ
-
-
1
Andreas Laner
0000036312
00036242
DNA
SEQ
-
-
1
Andreas Laner
0000036313
00036243
DNA
SEQ
-
-
1
Andreas Laner
0000036314
00036244
DNA
SEQ
-
-
1
Andreas Laner
0000036315
00036245
DNA
SEQ
-
-
1
Andreas Laner
0000036316
00036246
DNA
SEQ
-
-
1
Andreas Laner
0000036317
00036247
DNA
SEQ
-
-
1
Andreas Laner
0000036318
00036248
DNA
SEQ
-
-
1
Andreas Laner
0000036319
00036249
DNA
SEQ
-
-
1
Andreas Laner
0000036320
00036250
DNA
SEQ
-
-
1
Andreas Laner
0000039030
00038793
DNA
SEQ
-
-
1
Ruth Armstrong
0000046429
00046324
DNA
SEQ
-
-
1
kConFab - Heather Thorne
0000046433
00046328
DNA
SEQ
-
-
1
kConFab - Heather Thorne
0000047418
00047319
DNA
PTT;RT-PCR;SEQ
-
-
2
James Whitworth
0000047431
00047330
DNA
PTT;SEQ
-
-
2
James Whitworth
0000047432
00047331
DNA
SEQ
-
-
2
James Whitworth
0000048187
00048062
DNA
SEQ
-
-
2
James Whitworth
0000048188
00048063
DNA
SEQ
-
-
2
James Whitworth
0000048189
00048064
DNA
SEQ
-
-
2
James Whitworth
0000054697
00054750
DNA
SEQ-NG-I
-
-
2
Andreas Laner
0000057187
00057225
DNA
Southern
-
-
1
Johan den Dunnen
0000057188
00057226
DNA
Southern
-
-
1
Johan den Dunnen
0000111894
00111430
DNA
MLPA
-
-
1
Nancy Uhrhammer
0000174698
00173807
DNA
SEQ
-
-
1
Mamata Sivagnanam
0000177919
00177022
DNA
SEQ
-
-
1
Florence Coulet
0000184223
00183266
DNA
SEQ-NG-I
-
-
1
Andreas Laner
0000184236
00183277
DNA
SEQ
-
several exons risk genes
1
Johan den Dunnen
0000184237
00183278
DNA
SEQ
-
several exons risk genes
1
Johan den Dunnen
0000184498
00183530
DNA
SEQ
-
-
1
Gemeinschaftspraxis für Humangenetik Dresden
0000184506
00183538
DNA
SEQ
-
-
2
Elke Holinski-Feder
0000184507
00183539
DNA
SEQ
-
-
2
Elke Holinski-Feder
0000184612
00183644
DNA
SEQ-NG-I
buccal swab
-
2
Paul Iordache
0000184613
00183645
DNA
SEQ-NG-I
buccal swab
-
1
Paul Iordache
0000187849
00186881
DNA
SEQ
-
screen data 2013-01-01
1
Ruth Armstrong
0000187850
00186882
DNA
MLPA;SEQ
-
screen data 2013-01-01
1
Ruth Armstrong
0000187853
00186885
DNA
MLPA;SEQ
-
screen data 2012-01-01
2
Ruth Armstrong
0000187854
00186886
DNA
MLPA;SEQ
-
screen data 2012-01-01
1
Ruth Armstrong
0000187855
00186887
DNA
MLPA;SEQ
-
screen data 2011-01-01
1
Ruth Armstrong
0000187856
00186888
DNA
MLPA;SEQ
-
screen data 2012-01-01
1
Ruth Armstrong
0000187857
00186889
DNA
MLPA;SEQ
-
screen data 2011-01-01
1
Ruth Armstrong
0000187858
00186890
DNA
MLPA;SEQ
-
screen data 2010-01-01
1
Ruth Armstrong
0000187859
00186891
DNA
MLPA;SEQ
-
screen data 2007-01-01
1
Ruth Armstrong
0000187860
00186892
DNA
MLPA;SEQ
-
screen data 2010-01-01
1
Ruth Armstrong
0000187861
00186893
DNA
MLPA;SEQ
-
screen data 2007-01-01
1
Ruth Armstrong
0000187863
00186895
DNA
MLPA;SEQ
-
screen data 2009-01-01
1
Ruth Armstrong
0000187864
00186896
DNA
MLPA;SEQ
-
screen data 2010-01-01
1
Ruth Armstrong
0000187865
00186897
DNA
MLPA;SEQ
-
screen data 2004-01-01
1
Ruth Armstrong
0000187866
00186898
DNA
DGGE;SEQ
-
screen data 2001-01-01
2
Ruth Armstrong
0000187867
00186899
DNA
DGGE;SEQ
-
screen data 2002-01-01
2
Ruth Armstrong
0000187868
00186900
DNA
MLPA;SEQ
-
screen data 2008-01-01
1
Ruth Armstrong
0000187869
00186901
DNA
MLPA;SEQ
-
screen data 2009-01-01
1
Ruth Armstrong
0000187870
00186902
DNA
PCR;SEQ
-
screen data 2000-01-01
1
Ruth Armstrong
0000187876
00186908
DNA
SEQ;MLPA
-
screen data 2014-01-01
1
Ruth Armstrong
0000187877
00186909
DNA
Southern
-
-
1
Johan den Dunnen
0000187878
00186910
DNA
Southern
-
-
1
Johan den Dunnen
0000187879
00186911
DNA
SEQ
-
screen data 2000-01-01
1
InSiGHT - John-Paul Plazzer
0000187880
00186912
DNA
arrayCGH;SEQ
-
screen data 2015-01-01
1
InSiGHT - John-Paul Plazzer
0000187881
00186913
DNA
SEQ-NG-I;SEQ
-
-
1
Bryony A Thompson
0000187882
00186914
DNA
SEQ-NG-I;SEQ
-
-
1
Bryony A Thompson
0000187883
00186915
DNA
SEQ-NG-I;SEQ
-
-
1
Bryony A Thompson
0000187884
00186916
DNA
SEQ-NG-I;SEQ
-
-
2
Bryony A Thompson
0000187885
00186917
DNA
SEQ-NG-I;SEQ
-
-
1
Bryony A Thompson
0000187886
00186918
DNA
SEQ-NG-I;SEQ
-
-
1
Bryony A Thompson
0000187887
00186919
DNA
SEQ-NG-I;SEQ
-
-
1
Bryony A Thompson
0000187888
00186920
DNA
SEQ-NG-I;SEQ
-
-
1
Bryony A Thompson
0000187889
00186921
DNA
SEQ-NG-I;SEQ
-
-
1
Bryony A Thompson
0000187890
00186922
DNA
SEQ-NG-I;SEQ
-
-
1
Bryony A Thompson
0000187892
00186924
DNA
SEQ-NG
-
screen data 2015-11-01
1
InSiGHT - John-Paul Plazzer
0000187990
00187021
DNA
SEQ-NG
-
screen data 2015-08-17
1
InSiGHT - John-Paul Plazzer
0000187994
00187025
DNA
?
-
-
1
Elke Holinski-Feder
0000187995
00187026
DNA
?
-
-
1
Elke Holinski-Feder
0000188001
00187032
DNA
?
-
-
1
Ian Frayling
0000188002
00187033
DNA
?
-
-
1
Maurizio Genuardi
0000188003
00187034
DNA
?
-
-
1
Elke Holinski-Feder
0000188004
00187035
DNA
?
-
-
1
Elke Holinski-Feder
0000188049
00187080
DNA
PCR;SEQ
-
-
3
Peter Propping, Prof. Dr. med.
0000188050
00187081
DNA
PCR;SEQ
-
-
3
Peter Propping, Prof. Dr. med.
10 per page
25 per page
50 per page
100 per page
250 per page
500 per page
1000 per page
Legend
How to query
« First
Prev
1
2
3
4
5
6
7
8
9
10
11
...
Next
Last »
Powered by
LOVD v.3.0
Build 29
LOVD software ©2004-2023
Leiden University Medical Center