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MUTYH (mutY DNA glycosylase)
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Curator:
Instituto Nacional del Cancer
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Unique variants in the MUTYH gene
The variants shown are described using the
NM_001048171.1
NM_001128425.1
NM_001048174.1
NM_012222.3
transcript reference sequence.
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.
Effect
: The variant's effect on the function of the gene/protein, displayed in the format 'R/C'. R is the value reported by the source (publication, submitter) and this classification may vary between records. C is the value concluded by the curator. Note that in some database the curator uses Summary records to give details on the classification of the variant.Values used: '+' indicating the variant affects function, '+?' probably affects function, '-' does not affect function, '-?' probably does not affect function, '?' effect unknown, '.' effect was not classified.
Reported
: The number of times this variant has been reported in the database.
Exon
: Number of exon/intron containing variant; 2 = exon 2, 12i = intron 12, 2i_7i = exons 3 to 7, 8i_9 = border intron 8/exon 9.
DNA change (cDNA)
: Description of variant at DNA level, based on a coding DNA reference sequence (following HGVS recommendations); e.g. c.123C>T, c.123_145del, c.123_126dup.
Protein
: Description of variant at protein level (following HGVS recommendations).
p.(Arg345Pro) = change predicted from DNA (RNA not analysed)
p.Arg345Pro = change derived from RNA analysis
p.? = unknown effect
p.0? = probably no protein produced
Zygosity
: Homozygous or Heterozygous
All options:
Homo
Hetero
Not specified
Co_ocurrence
: If the variant is present in co-ocurrence with a mutation, please select the name of the mutated gene. If not, please select "no".
All options:
no
N/A
BRCA1
BRCA2
CHEK2
FANCC
MLH1
MSH2
MSH6
MUTYH
PALB2
PMS2
PTEN
APC
TP53
STK11
TSC1
RET
VHL
PALB2
NBN
CDKN2A
LZTR1
ATM
ERCC5
NF1
SDHB
BARD1
NTHL1
FANCC
BLM
BRIP1
RAD51C
GJB2
G6PC
SMN1
RNA change
: Description of variant at RNA level (following HGVS recommendations).
r.123c>u
r.? = unknown
r.(?) = RNA not analysed but probably transcribed copy of DNA variant
r.spl? = RNA not analysed but variant probably affects splicing
r.(spl?) = RNA not analysed but variant may affect splicing
r.0? = change expected to abolish transcription
Review status
: prueba
DNA change (genomic) (hg38)
: Description of variant at DNA level, based on the genomic DNA reference sequence (following HGVS recommendations).
g.12345678C>T
g.12345678_12345890del
g.12345678_12345890dup
Reference
: Reference to publication describing the variant, including links to OMIM (when available), PubMed or or other source, e.g. "den Dunnen ASHG2003 P2346".
DB-ID
: Database ID of variant, grouping multiple observations of the same variant together, starting with the HGNC gene symbol, followed by an underscore (_) and a six digit number (e.g. DMD_012345). _000000 is used for variants where DNA was not analysed (change predicted from RNA analysis), variants seen in animal models or variants not seen in humans but functionally tested in vitro.
dbSNP ID
: The dbSNP ID.
Variant remarks
: Remarks regarding the variant described, e.g. germline mosaicism in mother, 345 kb deletion, muscle RNA analysed, not in 200 control chromosomes tested, on founder haplotype, etc.
How to query this table
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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.
21 entries on 1 page. Showing entries 1 - 21.
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How to query
Effect
Reported
Exon
DNA change (cDNA)
Protein
Zygosity
Co_ocurrence
RNA change
Review status
DNA change (genomic) (hg38)
Reference
DB-ID
dbSNP ID
Variant remarks
Owner
-/-?, ?/-, -/-, ?/?, ./-?
11
2
c.64G>A
p.(Val22Met)
Hetero
MLH1, no, CHEK2, MSH6;CDKN2A
r.(?), r.(64g>a)
RECLASSIFIED NOVEMBER 2020
g.45334484C>T
-
MUTYH_000008
rs3219484
-
Lina Nuñez-Hospital Alemán
,
Maria Laura Gonzalez-Hospital Italiano
,
Claudia Martin-Hospital de Córdoba
,
Silvina Sisterna-Hospital de Comunidad
,
Pablo Kalfayan-Hospital Italiano
,
Pablo Kalfayan-CEMIC
+/+
1
2
c.85C>T
p.(Gln29*)
Hetero
MUTYH
r.(?)
-
g.45800135G>A
-
MUTYH_000001
rs768386527
-
Guillermo Alberto-Instituto Fleming
?/?
1
3
c.116-4G>A
p.?
Hetero
no
r.?
-
g.45333565C>T
-
MUTYH_000039
rs1064793421
-
Guillermo Alberto-Instituto Fleming
?/?
1
2
c.127_132delAACAGT
p.(Asn43_Ser44del)
Hetero
MLH1
r.(?)
-
g.45334416_45334421delACTGTT
-
MUTYH_000013
-
-
Florencia Petracchi-CEMIC
?/?
1
3
c.209A>G
p.(Tyr70Cys)
Hetero
no
r.(?)
-
g.45333510T>C
-
MUTYH_000011
-
-
Carlos Vaccaro-Hospital Italiano
-/-
26
6i, 4i
c.462+35A>G
p.(=)
Homo, Hetero
no, MLH1, MSH2, PMS2, MLH1, MUTYH, APC
r.(=)
-
g.45332883T>C
-
MUTYH_000003, MUTYH_000006
-
-
Pablo Kalfayan-Hospital Italiano
,
Florencia Petracchi-CEMIC
,
Lina Nuñez-Hospital Alemán
,
Carlos Vaccaro-Hospital Italiano
,
Maria Laura Gonzalez-Hospital Italiano
,
Lina Nuñez-Private Practice
,
Jose Llugdar-Instituto Oulton
,
Alejandra Mampel-Hospital Universitario de Mendoza
,
Pablo Kalfayan-CEMIC
,
Alejandra Mampel-COIR
?/?
1
8i
c.649-9C>T
p.(=)
Hetero
no
r.(=)
-
g.45332497G>A
-
MUTYH_000016
-
-
Norma Rossi-Hospital de Córdoba
+/+
1
9
c.721C>T
p.(Arg241Trp)
Hetero
CDH1
r.(?)
-
g.45332458G>A
-
MUTYH_000026
-
-
Guillermo Alberto-Instituto Fleming
+?/+?
1
10
c.842C>T
p.(Pro281Leu)
Hetero
no
r.(842c>u)
-
g.45332215G>A
-
MUTYH_000035
rs374950566
-
Silvina Sisterna-Hospital de Comunidad
?/?
2
10
c.883C>T
p.(Arg295Cys)
Hetero
BRCA1, no
r.(?)
-
g.45332174G>A
-
MUTYH_000015
rs138089183
-
Cecilia Montes-Hospital de Niños de la Santísima Trinidad
,
Claudia Martin-Hospital de Córdoba
?/?
1
10
c.934-2A>G
p.?
Hetero
no
r.?
-
g.45332088T>C
-
MUTYH_000036
rs77542170
-
Pablo Kalfayan-Hospital Italiano
+/+
1
12
c.956-1G>T
p.(?)
Hetero
BRCA2
r.(?)
-
g.
-
MUTYH_000028
-
-
Claudia Martin-Hospital de Córdoba
-/-, ./-
17
12
c.972G>C
p.(Gln324His)
Hetero, Homo, Not specified
no, APC, MSH2, MLH1, MUTYH, PMS2
r.(?)
-
g.45331833C>G
-
MUTYH_000004
-
-
Pablo Kalfayan-Hospital Italiano
,
Florencia Petracchi-CEMIC
,
Alejandra Mampel-Hospital Universitario de Mendoza
,
Silvina Sisterna-Hospital de Comunidad
,
Lina Nuñez-Private Practice
,
Carlos Vaccaro-Hospital Italiano
,
Jose Llugdar-Instituto Oulton
+/+?, +/+
2
13
c.1103G>A
p.Gly368Asp
Hetero
BRCA2, N/A
r.?
-
g.45331556C>T
-
MUTYH_000010
rs36053993
(2 VUS (FANCA and XRCC2) Not yet submitted
Laura Vargas Roig-IMBECU
,
Guillermo Alberto-Instituto Fleming
?/?
1
13
c.1234C>T
p.(Arg412Cys)
Hetero
no
r.(?)
-
g.45331467G>A
-
MUTYH_000012
-
-
Alejandra Mampel-Hospital Universitario de Mendoza
?/?
1
13
c.1259C>T
p.(Thr420Met)
Hetero
no
r.(?)
-
g.45331442G>A
-
MUTYH_000023
-
-
Claudia Martin-Hospital de Córdoba
./-?
1
14
c.1389G>C
p.(=)
Hetero
no
r.(=)
-
g.45331227C>G
-
MUTYH_000019
-
-
Silvina Sisterna-Hospital de Comunidad
-/-
27
14i
c.1435-40C>G
p.(=)
Homo, Hetero
no, MLH1, MSH2, PMS2, MLH1, MUTYH, APC
r.(=)
-
g.45330597G>C
-
MUTYH_000005
-
-
Pablo Kalfayan-Hospital Italiano
,
Florencia Petracchi-CEMIC
,
Lina Nuñez-Hospital Alemán
,
Carlos Vaccaro-Hospital Italiano
,
Maria Laura Gonzalez-Hospital Italiano
,
Lina Nuñez-Private Practice
,
Jose Llugdar-Instituto Oulton
,
Alejandra Mampel-Hospital Universitario de Mendoza
,
Pablo Kalfayan-CEMIC
,
Alejandra Mampel-COIR
-?/-?
1
16
c.1502C>T
p.(Ser501Phe)
Hetero
no
r.(?)
-
g.45329412G>A
-
MUTYH_000018
-
-
Laura Vargas Roig-IMBECU
./?
1
16
c.1530G>A
p.(Met510Ile)
Hetero
no
r.(?)
-
g.45329384C>T
-
MUTYH_000007
-
-
Pablo Kalfayan-Hospital Italiano
?/?
1
16
c.1546G>T
p.(Asp516Tyr)
Hetero
no
r.(1546g>u)
-
g.45329368C>A
-
MUTYH_000034
rs147923905
-
Pablo Kalfayan-Hospital Italiano
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