Global Variome shared LOVD
FANCM (Fanconi anemia, complementation group M)
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
Curator:
Arleen D. Auerbach
View all genes
View FANCM gene homepage
View graphs about the FANCM gene database
Create a new gene entry
View all transcripts
View all transcripts of gene FANCM
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene FANCM
View all variants in gene FANCM
Full data view for gene FANCM
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 FANCM
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene FANCM
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene FANCM
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
All screenings for gene FANCM
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
arrayMET = array for methylation analysis
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 = single 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.
1512 entries on 16 pages. Showing entries 1 - 100.
10 per page
25 per page
50 per page
100 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
0000001418
00001617
DNA
SEQ;SEQ-NG-I
-
-
1
Najim Ameziane
0000020024
00020027
DNA;RNA
RT-PCR;SEQ
-
-
4
Arleen D. Auerbach
0000020025
00020028
DNA
SEQ
-
-
2
Arleen D. Auerbach
0000020026
00020029
DNA
SEQ
-
-
2
Ashot Harutyunyan
0000020027
00020030
DNA
SEQ
-
-
1
Christopher Smith
0000247629
00246517
DNA
SEQ
-
gene panel
1
Florentia Fostira
0000247630
00246518
DNA
SEQ
-
gene panel
1
Florentia Fostira
0000261977
00260872
DNA
SEQ
-
-
1
Johan den Dunnen
0000261978
00260873
DNA
SEQ
-
-
1
Johan den Dunnen
0000261979
00260874
DNA
SEQ
-
-
1
Johan den Dunnen
0000261980
00260875
DNA
SEQ
-
-
1
Johan den Dunnen
0000261981
00260876
DNA
SEQ
-
-
1
Johan den Dunnen
0000261982
00260877
DNA
SEQ
-
-
1
Johan den Dunnen
0000261983
00260878
DNA
SEQ
-
-
1
Johan den Dunnen
0000261984
00260880
DNA
SEQ;SEQ-NG
-
WES
4
Johan den Dunnen
0000261985
00260881
DNA
SEQ;SEQ-NG
-
WES
1
Johan den Dunnen
0000261986
00260882
DNA
SEQ;SEQ-NG
-
WES
1
Johan den Dunnen
0000261988
00260884
DNA
SEQ;SEQ-NG
-
WES
1
Johan den Dunnen
0000261990
00260885
DNA
SEQ;SEQ-NG
-
WES
1
Johan den Dunnen
0000337404
00336174
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337405
00336175
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337406
00336176
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337407
00336177
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337408
00336178
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337409
00336179
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337410
00336180
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337411
00336181
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337412
00336182
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337413
00336183
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337414
00336184
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337415
00336185
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337416
00336186
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337536
00336306
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337537
00336307
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337539
00336309
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337540
00336310
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337541
00336311
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337542
00336312
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000337543
00336313
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339943
00338713
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339944
00338714
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339945
00338715
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339946
00338716
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339947
00338717
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339948
00338718
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339949
00338719
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339950
00338720
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339951
00338721
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339952
00338722
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339953
00338723
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339954
00338724
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339955
00338725
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339956
00338726
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339957
00338727
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339958
00338728
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339959
00338729
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339960
00338730
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339961
00338731
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339962
00338732
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339963
00338733
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339964
00338734
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339965
00338735
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339966
00338736
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339967
00338737
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339968
00338738
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339969
00338739
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339970
00338740
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339971
00338741
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339972
00338742
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339973
00338743
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339974
00338744
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339975
00338745
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339976
00338746
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339977
00338747
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339978
00338748
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339979
00338749
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339980
00338750
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339981
00338751
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339982
00338752
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339983
00338753
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339984
00338754
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339985
00338755
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339986
00338756
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339987
00338757
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339988
00338758
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339989
00338759
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339990
00338760
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339991
00338761
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339992
00338762
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339993
00338763
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339994
00338764
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339995
00338765
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339996
00338766
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339997
00338767
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339998
00338768
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000339999
00338769
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000340000
00338770
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000340001
00338771
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000340002
00338772
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
0000340003
00338773
DNA
SEQ-NG
-
34-gene panel
1
BRIDGES consortium
10 per page
25 per page
50 per page
100 per page
Legend
How to query
« First
Prev
1
2
3
4
5
6
7
8
9
10
11
...
Next
Last »
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our
APIs
to retrieve data.
Powered by
LOVD v.3.0
Build 30b
LOVD software ©2004-2024
Leiden University Medical Center
Database contents © by their respective submitters and curators