Global Variome shared LOVD
SLC26A4 (solute carrier family 26, member 4)
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]
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Curator:
David Baux
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Unique variants in the SLC26A4 gene
This database is one of the
”Retinal and hearing impairment genetic variant databases”
.
The variants shown are described using the NM_000441.1 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 = from intron 2 to intron 7, 8i_9 = intron 8/exon 9 boundary, _1 = 5' to exon 1, 18_ = 3' of exon 18, _1_18_ = encompassing the entire 18-exon gene
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. For deletions/duplications extending beyond the reference transcript resp. {0}/{2} is used to replace del/dup. Extent of the deletion/duplication should be specified using the genomic description (g.). "-" indicates the variant described on genomic level does not affect the coding DNA reference sequence.
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
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
Classification method
: The method used for the clinical classification of this variant.
All options:
ACMG
ACGS
EAHAD-CFDB
ENIGMA
IARC
InSiGHT
kConFab
other
Clinical classification
: Clinical classification of variant, preferably based on standardised criteria (e.g. ACMG), directed on the clinical consequences as published/submitted, indicated using an enriched system including inheritance: e.g. pathogenic, pathogenic (dominant), pathogenic (recessive), pathogenic (!), pathogenic (maternal), pathogenic (paternal). Standard inheritance is covered by dominant/recessive, imprinting by maternal/paternal. A '!' warns for exceptional circumstances to be explained in the 'Remarks' field (low penetrance, variants pathogenic in heterozygous state only, hypomorphic/hypermorphic variants, protective variants, etc.). Non-disease consequences (e.g. drug metabolism (pharmacogenetics), risk factor, blood group, tasting bitter) are indicated using additions to the benign classification; benign (dominant), benign (recessive), benign (!), etc. The value 'association' is used for variants associated with a phenotype and 'NA' for variants from in vitro/in silico records. NOTE: classification may differ from the opinion of the curator as given in a variant SUMMARY-record or the 'Functional effect concluded'). NOTE: pathogenic/likely pathogenic should go together with "variant (probably) affects function" In ClassFunctional.
All options:
pathogenic
pathogenic (dominant)
pathogenic (recessive)
pathogenic (!)
pathogenic (maternal)
pathogenic (paternal)
likely pathogenic
likely pathogenic (dominant)
likely pathogenic (recessive)
likely pathogenic (!)
likely pathogenic (maternal)
likely pathogenic (paternal)
VUS
VUS (!)
likely benign
likely benign (dominant)
likely benign (recessive)
likely benign (!)
likely benign (maternal)
likely benign (paternal)
benign
benign (dominant)
benign (recessive)
benign (!)
benign (maternal)
benign (paternal)
conflicting
association
NA
DNA change (genomic) (hg19)
: HGVS description of variant at DNA level, based on the genomic (chromosomal) DNA reference sequence; e.g. g.12345678C>T, g.12345679del, g.12345678_12345890dup
DNA change (hg38)
: HGVS description of variant at DNA level, based on the hg38 genomic (chromosomal) eference sequence; e.g. g.12345678C>T, g.12345679del, g.12345678_12345890dup
Published as
: listed only when different from "DNA change"; variant as reported originally (e.g. 521delT). Variants seen in animal models, tested in vitro, predicted from RNA analysis, etc. are described between brackets like c.(456C>G)
ISCN
: description of the variant according to ISCN nomenclature
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
Variant remarks
: remarks regarding variant described, e.g. germline mosaicism in mother, 345 kb deletion, muscle RNA analysed, not in 200 control chromosomes tested, on founder haplotype, etc.
Reference
: publication describing the variant submitted, incl. links to OMIM, PubMed or other source, e.g. "den Dunnen ASHG2003 P2346"
ClinVar ID
: ID of variant in ClinVar database
dbSNP ID
: the dbSNP ID
Origin
: Origin of variant/record: Germline = in all cells, De novo = in all cells, but not in either parent, Germline/De novo (untested) = in all cells, parents not tested (use only when De novo is likely, e.g. isolated/sporadic cases with dominant disease), Somatic = present in a subset of cells, but not in either parent, Uniparental disomy = from parental disomy (maternal or paternal), CLASSIFICATION record = submitter only sharing variant classification (note another report may share Individual data), SUMMARY record = master summary record from curator (may link to another database), In vitro (cloned) = data resulting from in vitro functional assays, animal model = data from animal model, Artefact = false positive variant call, DUPLICATE record = variant already described on another chromosome (e.g. unbalanced translocation, duplicating transposition, 2nd fusion transcript, etc.)
All options:
Germline
De novo
Germline/De novo (untested)
Somatic
Uniparental disomy
Uniparental disomy, maternal allele
Uniparental disomy, paternal allele
CLASSIFICATION record
SUMMARY record
In vitro (cloned)
In silico
animal model
Artefact
DUPLICATE record
Unknown
Not applicable
Segregation
: Indicates whether the variant segregates with the phenotype (yes), does not segregate with the phenotype (no) or segregation is unknown (?)
All options:
? = unknown
yes = segregates with phenotype
no = does not segregate with phenotype
- = not applicable
Frequency
: frequency in which the variant was found; e.g 5/760 chromosomes (in 5 of 760 chromosomes tested), 1/33 patients (in 1 of 33 patients analysed in study), 0.05 controls (in 5% of control cases tested)
Re-site
: restriction enzyme recognition site created (+) or destroyed (-); e.g. BglII+;BamHI-
VIP
: variant VIP-status was requested for matchmaking - need collaboration(s) to crack the case - please contact the submitter/curator. NOTE: to get VIP status ask the curator.
Methylation
: result of methylation test; GOM (gain of methylation), LOM (loss of methylation), 30% (30% methylated). NOTE: when several tests were done mention the method as well (e.g. MS-PCR 75%)
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.
250 entries on 3 pages. Showing entries 1 - 100.
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Effect
Reported
Exon
DNA change (cDNA)
RNA change
Protein
Classification method
Clinical classification
DNA change (genomic) (hg19)
DNA change (hg38)
Published as
ISCN
DB-ID
Variant remarks
Reference
ClinVar ID
dbSNP ID
Origin
Segregation
Frequency
Re-site
VIP
Methylation
Owner
+/.
1
_1_3i
c.-1288_304+3801del
r.0?
p.0?
-
pathogenic (recessive)
g.107300016_107307681del
g.107659571_107667236del
g.-1066C_6602Adel
-
SLC26A4_000285
-
PubMed: Lin 2019
,
PubMed: Wu 2019
-
-
Germline
-
-
-
-
-
Johan den Dunnen
?/.
1
-
c.-109G>A
r.(?)
p.(=)
-
VUS
g.107301195G>A
g.107660750G>A
-
-
SLC26A4_000154
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/+, ?/.
14
1
c.-103T>C
r.(0?), r.(?)
p.(0?), p.(=)
-
NA, pathogenic, VUS
g.107301201T>C
g.107660756T>C
SLC26A4(NM_000441.1):c.-103T>C
-
SLC26A4_000127, SLC26A4_000197
heterozygous; may affect transcription (Yang ,2007), not in 200 control chromosomes,
3 more items
PubMed: B.Choi 2009
,
PubMed: Baux, Vaché 2017
,
PubMed: Yang 2007
,
Journal: Yang 2007
-
rs60284988
CLASSIFICATION record, Germline, In vitro (cloned)
-
0/146 controls, 1/429 cases
-
-
-
Johan den Dunnen
,
VKGL-NL_Rotterdam
,
VKGL-NL_Nijmegen
,
Anne-Françoise Roux
-/-, -/.
2
1
c.-66C>G
r.(=), r.(?)
p.(=)
ACMG
benign
g.107301238C>G
g.107660793C>G
SLC26A4(NM_000441.1):c.-66C>G
-
SLC26A4_000122, SLC26A4_000201
heterozygous; No pathogenicity, VKGL data sharing initiative Nederland
PubMed: B.Choi 2009
-
rs17154282
CLASSIFICATION record, Germline
-
0/146 controls
-
-
-
VKGL-NL_Rotterdam
,
Anne-Françoise Roux
?/?
1
1
c.-60A>G
r.(?)
p.(=)
ACMG
VUS
g.107301244A>G
g.107660799A>G
-
-
SLC26A4_000126
1 more item
PubMed: B.Choi 2009
-
-
Germline
-
0/146 controls
-
-
-
Anne-Françoise Roux
+?/.
1
-
c.-3-2A>G
r.spl?
p.?
-
likely pathogenic
g.107302082A>G
g.107661637A>G
-
-
SLC26A4_000230
1 heterozygous, no homozygous;
Clinindb (India)
PubMed: Narang 2020
,
Journal: Narang 2020
-
rs397516411
Germline
-
1/2795 individuals
-
-
-
Mohammed Faruq
+/+, +/.
5
2
c.2T>C
r.(?)
p.(Met1?), p.Met1Thr
-
pathogenic
g.107302088T>C
g.107661643T>C
SLC26A4(NM_000441.1):c.2T>C (p.M1?),
2 more items
-
SLC26A4_000049, SLC26A4_000202
heterozygous; Mutation, heterozygous; Pathogenic, VKGL data sharing initiative Nederland
PubMed: B.Choi 2009
; USMA-
missense variant in MSV3d
,
2 more items
-
rs111033302
CLASSIFICATION record, Germline
-
0/192 controls, 0/400 controls
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_Nijmegen
,
Anne-Françoise Roux
+/.
2
-
c.2T>G
r,(?), r.(?)
p.(Met1?), p.?
-
pathogenic, pathogenic (recessive)
g.107302088T>G
g.107661643T>G
(M1R)
-
SLC26A4_000281
combination of alleles not reported, VKGL data sharing initiative Nederland
PubMed: Wu 2019
-
-
CLASSIFICATION record, Germline
-
1/1291 cases hearing loss
-
-
-
Johan den Dunnen
,
VKGL-NL_Nijmegen
-/.
1
-
c.15C>A
r.(?)
p.(Gly5=)
-
benign
g.107302101C>A
g.107661656C>A
SLC26A4(NM_000441.2):c.15C>A (p.G5=)
-
SLC26A4_000210
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
-?/.
1
-
c.17G>T
r.(?)
p.(Gly6Val)
-
likely benign
g.107302103G>T
-
SLC26A4(NM_000441.2):c.17G>T (p.G6V)
-
SLC26A4_000253
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
-?/.
1
-
c.28C>A
r.(?)
p.(Pro10Thr)
-
likely benign
g.107302114C>A
-
SLC26A4(NM_000441.1):c.28C>A (p.P10T)
-
SLC26A4_000239
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+/.
1
-
c.42del
r.(?)
p.(Glu15SerfsTer51)
ACMG
pathogenic (recessive)
g.107302128del
g.107661683del
42delC
-
SLC26A4_000268
-
PubMed: Richard 2019
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
2
-
c.71G>T
r.(?)
p.(Arg24Leu)
-
pathogenic (recessive)
g.107302157G>T
g.107661712G>T
-
-
SLC26A4_000269
-
PubMed: Richard 2019
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+?/?
1
2
c.84C>A
r.(?)
p.(Ser28Arg)
ACMG
VUS
g.107302170C>A
g.107661725C>A
-
-
SLC26A4_000111
heterozygous; Mutation
PubMed: M.Ladsous 2014
; USMA-
missense variant in MSV3d
-
-
Germline
-
-
-
-
-
Anne-Françoise Roux
+/+, +/.
9
2
c.85G>C
r.(85g>c), r.(?)
p.(Glu29Gln)
-
pathogenic
g.107302171G>C
g.107661726G>C
G29Q, Pathogeni Functional studies showed reduced activity of mutant pendrin (A.Pera et al.,2008),
1 more item
-
SLC26A4_000083
heterozygous; Mutation, heterozygous; Pathogenic, heterozygous; UV3,
2 more items
PubMed: A.Pera 2008
; USMA-
missense variant in MSV3d
,
PubMed: Yang 2007
,
Journal: Yang 2007
,
3 more items
-
rs111033205
CLASSIFICATION record, Germline
yes
1/428 controls
-
-
-
Johan den Dunnen
,
VKGL-NL_Rotterdam
,
VKGL-NL_Nijmegen
,
Anne-Françoise Roux
-?/.
1
-
c.135G>T
r.(?)
p.(Thr45=)
-
likely benign
g.107302221G>T
g.107661776G>T
SLC26A4(NM_000441.1):c.135G>T (p.T45=)
-
SLC26A4_000234
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+/.
1
-
c.142G>T
r.(?)
p.(Glu48Ter)
-
pathogenic
g.107302228G>T
g.107661783G>T
SLC26A4(NM_000441.1):c.142G>T (p.E48*)
-
SLC26A4_000203
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+/.
1
-
c.154A>T
r.(?)
p.(Lys52Ter)
ACMG
pathogenic (recessive)
g.107302240A>T
g.107661795A>T
-
-
SLC26A4_000270
-
PubMed: Richard 2019
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
-
c.164+1G>C
r.spl
p.?
-
pathogenic (recessive)
g.107302251G>C
g.107661806G>C
-
-
SLC26A4_000289
combination of alleles not reported
PubMed: Wu 2019
-
-
Germline
-
4/1291 cases hearing loss
-
-
-
Johan den Dunnen
+/+
1
2i
c.164+2T>C
r.spl?
p.?
-
pathogenic (recessive)
g.107302252T>C
g.107661807T>C
-
-
SLC26A4_000138
homozygous
PubMed: Baux, Vaché 2017
-
rs397516420
Germline
-
-
-
-
-
Anne-Françoise Roux
+/+
1
2i
c.165-2A>G
r.spl?
p.?
-
pathogenic
g.107303739A>G
g.107663294A>G
-
-
SLC26A4_000066
heterozygous; Mutation
PubMed: López-Bigas N 2002
-
-
Germline
-
-
-
-
-
Anne-Françoise Roux
+/.
1
-
c.170C>A
r.(?)
p.(Ser57Ter)
-
pathogenic (recessive)
g.107303746C>A
g.107663301C>A
-
-
SLC26A4_000271
-
PubMed: Park 2003
,
PubMed: Naz 2017
-
rs111033200
Germline
-
-
-
-
-
Johan den Dunnen
-?/.
1
-
c.187G>A
r.(?)
p.(Gly63Ser)
-
likely benign
g.107303763G>A
g.107663318G>A
SLC26A4(NM_000441.1):c.187G>A (p.G63S)
-
SLC26A4_000227
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
?/.
1
-
c.200C>G
r.(?)
p.(Thr67Ser)
-
VUS
g.107303776C>G
g.107663331C>G
-
-
SLC26A4_000211
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+?/.
1
-
c.203T>C
r.(?)
p.(Leu68Pro)
-
likely pathogenic
g.107303779T>C
-
-
-
SLC26A4_000258
-
-
-
rs749712560
CLASSIFICATION record
-
-
-
-
-
MobiDetails
?/.
1
-
c.209C>T
r.(?)
p.(Pro70Leu)
-
VUS
g.107303785C>T
-
-
-
SLC26A4_000282
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/+
1
3
c.218del
r.(?)
p.(Glu73Glyfs*24)
-
pathogenic
g.107303794del
g.107663349del
-
-
SLC26A4_000056
heterozygous; Mutation
PubMed: Huang S 2011
-
-
Germline
-
0/400 controls
-
-
-
Anne-Françoise Roux
+/.
1
-
c.230A>T
r,(?)
p.(Lys77Ile)
-
pathogenic (recessive)
g.107303806A>T
g.107663361A>T
-
-
SLC26A4_000290
combination of alleles not reported
PubMed: Wu 2019
-
-
Germline
-
1/1291 cases hearing loss
-
-
-
Johan den Dunnen
+/.
1
-
c.235C>T
r,(?)
p.(Arg79Ter)
-
pathogenic (recessive)
g.107303811C>T
g.107663366C>T
-
-
SLC26A4_000291
combination of alleles not reported
PubMed: Wu 2019
-
-
Germline
-
1/1291 cases hearing loss
-
-
-
Johan den Dunnen
+/., +?/.
2
-
c.241A>G
r,(?), r.(?)
p.(Lys81Glu)
ACMG
likely pathogenic (recessive), pathogenic (recessive)
g.107303817A>G
g.107663372A>G
-
-
SLC26A4_000287
ACMG PM2, PM3, PP3, PP4, combination of alleles not reported
PubMed: Lin 2019
,
PubMed: Wu 2019
-
-
Germline
-
1/1291 cases hearing loss
-
-
-
Johan den Dunnen
-/-
1
3
c.262G>A
r.(?)
p.(Val88Ile)
-
benign
g.107303838G>A
g.107663393G>A
-
-
SLC26A4_000129
1 more item
PubMed: A.Pera 2008
; USMA-
missense variant in MSV3d
-
-
Germline
-
1/428 controls
-
-
-
Anne-Françoise Roux
+/+
1
3
c.279del
r.(?)
p.(Ser93Argfs*4)
-
pathogenic
g.107303855del
g.107663410del
-
-
SLC26A4_000077
heterozygous; Pathogenic
PubMed: V.de Moraes 2013
-
-
Germline
-
0/60 controls
-
-
-
Anne-Françoise Roux
+?/+?
1
3
c.281C>T
r.(?)
p.(Thr94Ile)
ACMG
VUS
g.107303857C>T
g.107663412C>T
-
-
SLC26A4_000041
heterozygous; Mutation
PubMed: Huang S 2011
; USMA-
missense variant in MSV3d
-
-
Germline
-
0/400 controls
-
-
-
Anne-Françoise Roux
+/.
1
-
c.304G>A
r.(?)
p.(Gly102Arg)
-
pathogenic
g.107303880G>A
-
-
-
SLC26A4_000241
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+?/.
1
-
c.304G>C
r.(?)
p.(Gly102Arg)
-
likely pathogenic
g.107303880G>C
-
-
-
SLC26A4_000283
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/+
2
3i_6i
c.304+292_765+2672del
r.?
p.(Gly102Aspfs*4)
-
pathogenic
g.107304172_107318226del
g.107663727_107677781del
Pathogenic, intragenic deletion of 14052kb
-
SLC26A4_000134
heterozygous; Pathogenic
PubMed: A.Pera 2008
-
-
Germline
-
0/428 controls
-
-
-
Anne-Françoise Roux
+?/?
2
4
c.317C>A
r.(?)
p.(Ala106Asp)
ACMG
VUS
g.107312595C>A
g.107672150C>A
-
-
SLC26A4_000084
heterozygous; Mutation
PubMed: C.Campbell 2001
; USMA-
missense variant in MSV3d
-
-
Germline
-
-
-
-
-
Anne-Françoise Roux
+?/.
1
-
c.317C>T
r.(?)
p.(Ala106Val)
ACMG
likely pathogenic (recessive)
g.107312595C>T
g.107672150C>T
-
-
SLC26A4_000272
-
PubMed: Richard 2019
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/+
2
4
c.322del
r.(?)
p.(Leu108*)
-
pathogenic
g.107312600del
g.107672155del
-
-
SLC26A4_000099
heterozygous; Likely pathogenic mutation, heterozygous; Pathogenic
PubMed: K.Tsukamoto 2003
,
PubMed: S.Iwasaki 2006
-
-
Germline
-
0/192 controls
-
-
-
Anne-Françoise Roux
?/.
1
-
c.334C>T
r.(?)
p.(Pro112Ser)
-
VUS
g.107312612C>T
-
-
-
SLC26A4_000254
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
?/.
2
-
c.347G>A
r.(?)
p.(Gly116Asp)
-
VUS
g.107312625G>A
g.107672180G>A
SLC26A4(NM_000441.1):c.347G>A (p.G116D)
-
SLC26A4_000212
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_Nijmegen
+/.
3
4
c.349C>T
r.(?)
p.(Leu117Phe)
-
pathogenic
g.107312627C>T
g.107672182C>T
-
-
SLC26A4_000192
found in 1/50 controls (Ashkenazi); not found among ~4000 non-Ashkenazi Jews,
1 more item
-
-
-
Germline
yes
5/316 cases (hom), 1/316 cases (het)
-
-
-
Zippi Brownstein
+?/?
1
4
c.367C>T
r.(?)
p.(Pro123Ser)
ACMG
VUS
g.107312645C>T
g.107672200C>T
-
-
SLC26A4_000095
heterozygous; Likely pathogenic mutation
PubMed: K.Tsukamoto 2003
; USMA-
missense variant in MSV3d
-
-
Germline
-
0/192 controls
-
-
-
Anne-Françoise Roux
+/.
1
-
c.370_382del
r.(?)
p.(Ile124Leufs*17)
-
pathogenic
g.107312648_107312660del
-
-
-
SLC26A4_000242
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/.
1
-
c.387del
r,(?)
p.(Phe130LeufsTer15)
-
pathogenic (recessive)
g.107312665del
g.107672220del
387delC
-
SLC26A4_000292
combination of alleles not reported
PubMed: Wu 2019
-
-
Germline
-
1/1291 cases hearing loss
-
-
-
Johan den Dunnen
+?/?
1
4
c.395C>T
r.(?)
p.(Thr132Ile)
ACMG
VUS
g.107312673C>T
g.107672228C>T
-
-
SLC26A4_000065
heterozygous; Mutation
PubMed: López-Bigas N 2002
; USMA-
missense variant in MSV3d
-
-
Germline
-
-
-
-
-
Anne-Françoise Roux
+/+
1
4
c.398C>A
r.(?)
p.(Ser133*)
-
pathogenic
g.107312676C>A
g.107672231C>A
-
-
SLC26A4_000119
heterozygous; Mutation
PubMed: M.Ladsous 2014
; USMA-
missense variant in MSV3d
-
-
Germline
-
-
-
-
-
Anne-Françoise Roux
?/.
1
-
c.404A>G
r.(?)
p.(His135Arg)
-
VUS
g.107312682A>G
g.107672237A>G
-
-
SLC26A4_000228
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/+
1
4
c.407_411del
r.(?)
p.(Ile136Serfs*44)
-
pathogenic
g.107312685_107312689del
g.107672240_107672244del
406del5 (FS135/X179)
-
SLC26A4_000070
heterozygous; Pathogenic
PubMed: López-Bigas N 2002
-
-
Germline
-
-
-
-
-
Anne-Françoise Roux
+/+, +/., +?/.
14
4
c.412G>T
r.(?)
p.(Val138Phe)
ACMG
likely pathogenic, pathogenic, pathogenic (recessive)
g.107312690G>T
g.107672245G>T
Pathogenic, functional studies showed no activity of mutant pendrin (Taylor JP et al;2002)
-
SLC26A4_000072, SLC26A4_000155
compound heterozygous, heterozygous; loss of function mutation (Taylor ,2002); Pathogenic,
3 more items
PubMed: A.Pera 2008
; USMA-
missense variant in MSV3d
,
PubMed: Batissoco 2021
,
4 more items
ClinVar-SCV001792213
,
ClinVar-4835
rs111033199
,
rs111033313
CLASSIFICATION record, Germline
yes
0/200 controls, 0/428 controls, 0/60 controls
-
-
-
VKGL-NL_Nijmegen
,
Anne-Françoise Roux
,
MobiDetails
,
Karina Lezirovitz Mandelbaum
+/.
1
-
c.413T>A
r.(?)
p.(Val138Asp)
-
pathogenic (recessive)
g.107312691T>A
g.107672246T>A
-
-
SLC26A4_000273
-
PubMed: Richard 2019
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/+
1
4
c.414del
r.(?)
p.(Gly139Aspfs*6)
-
pathogenic
g.107312692del
g.107672247del
-
-
SLC26A4_000052
heterozygous; Mutation
PubMed: Huang S 2011
-
-
Germline
-
0/400 controls
-
-
-
Anne-Françoise Roux
-/.
1
-
c.416-16G>T
r.(=)
p.(=)
-
benign
g.107314593G>T
g.107674148G>T
SLC26A4(NM_000441.2):c.416-16G>T
-
SLC26A4_000229
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
-/.
2
-
c.416-13T>C
r.(=)
p.(=)
-
benign
g.107314596T>C
g.107674151T>C
SLC26A4(NM_000441.1):c.416-13T>C, SLC26A4(NM_000441.2):c.416-13T>C
-
SLC26A4_000204
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_AMC
+/.
2
-
c.416-1G>A
r.spl, r.spl?
p.?
-
pathogenic, pathogenic (recessive)
g.107314608G>A
g.107674163G>A
-
-
SLC26A4_000213
combination of alleles not reported, VKGL data sharing initiative Nederland
PubMed: Wu 2019
-
-
CLASSIFICATION record, Germline
-
1/1291 cases hearing loss
-
-
-
Johan den Dunnen
,
VKGL-NL_Nijmegen
+/.
2
-
c.416G>C
r.(?)
p.(Gly139Ala)
-
pathogenic
g.107314609G>C
g.107674164G>C
SLC26A4(NM_000441.1):c.416G>C (p.G139A)
-
SLC26A4_000156
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_Nijmegen
+/.
1
-
c.416G>T
r.(?)
p.(Gly139Val)
-
pathogenic (recessive)
g.107314609G>T
g.107674164G>T
-
-
SLC26A4_000274
-
PubMed: Richard 2019
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+?/?
1
5
c.425C>T
r.(?)
p.(Pro142Leu)
ACMG
VUS
g.107314618C>T
g.107674173C>T
-
-
SLC26A4_000076
heterozygous; Expected impairment of pendrin function
PubMed: V.de Moraes 2013
; USMA-
missense variant in MSV3d
-
-
Germline
-
0/60 controls
-
-
-
Anne-Françoise Roux
?/.
1
-
c.431T>C
r.(?)
p.(Val144Ala)
-
VUS
g.107314624T>C
g.107674179T>C
SLC26A4(NM_000441.2):c.431T>C (p.V144A)
-
SLC26A4_000214
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
+/., +?/?
3
5
c.439A>G
r,(?), r.(?)
p.(Met147Val)
ACMG
pathogenic (recessive), VUS
g.107314632A>G
g.107674187A>G
-
-
SLC26A4_000059, SLC26A4_000100
combination of alleles not reported, heterozygous; Likely pathogenic mutation, heterozygous; Mutation
PubMed: Huang S 2011
; USMA-
missense variant in MSV3d
,
PubMed: Wu 2019
,
1 more item
-
-
Germline
-
0/192 controls, 0/400 controls, 2/1291 cases hearing loss
-
-
-
Johan den Dunnen
,
Anne-Françoise Roux
+?/?, ?/.
2
5
c.446G>A
r.(?)
p.(Gly149Glu)
ACMG
VUS
g.107314639G>A
g.107674194G>A
p.(G149R)
-
SLC26A4_000074
heterozygous; Expected impairment of pendrin function, VKGL data sharing initiative Nederland
PubMed: V.de Moraes 2013
; USMA-
missense variant in MSV3d
-
-
CLASSIFICATION record, Germline
-
0/60 controls
-
-
-
VKGL-NL_Nijmegen
,
Anne-Françoise Roux
+/+
10
5
c.451del
r.(?)
p.(Val151Leufs*3)
-
pathogenic
g.107314644del
g.107674199del
-
-
SLC26A4_000010
homozygous; Pathogenic
PubMed: Ben Said 2012
-
-
Germline
-
0/100 controls
-
-
-
Anne-Françoise Roux
+?/.
1
-
c.471C>T
r.(?)
p.(Pro157=)
-
likely pathogenic
g.107314664C>T
-
-
-
SLC26A4_000260
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/.
1
-
c.481T>A
r.(?)
p.(Phe161Ile)
ACMG
likely pathogenic (recessive)
g.107314674T>A
-
-
-
SLC26A4_000248
in compound heterozygosis with c.1615-2A>G
PubMed: Batissoco 2021
ClinVar-SCV001792216
-
Germline
yes
-
-
-
-
Karina Lezirovitz Mandelbaum
+/+
1
5
c.496del
r.(?)
p.(Ser166Alafs*6)
-
pathogenic
g.107314689del
g.107674244del
-
-
SLC26A4_000044
heterozygous; Mutation
PubMed: Huang S 2011
-
-
Germline
-
0/400 controls
-
-
-
Anne-Françoise Roux
+?/.
1
-
c.505del
r.(?)
p.(Thr169Leufs*3)
-
likely pathogenic
g.107314698del
g.107674253del
-
-
SLC26A4_000198
-
PubMed: Zazo Seco 2017
,
Journal: Zazo Seco 2017
-
-
Germline
-
-
-
-
-
Mieke Wesdorp
-?/.
1
-
c.523A>G
r.(?)
p.(Met175Val)
-
likely benign
g.107314716A>G
g.107674271A>G
SLC26A4(NM_000441.2):c.523A>G (p.M175V)
-
SLC26A4_000235
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
-?/.
1
-
c.535G>A
r.(?)
p.(Ala179Thr)
-
likely benign
g.107314728G>A
-
SLC26A4(NM_000441.1):c.535G>A (p.A179T)
-
SLC26A4_000261
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+/., +?/.
3
5
c.554G>C
r.(?)
p.(Arg185Thr)
ACMG
pathogenic, pathogenic (recessive)
g.107314747G>C
g.107674302G>C
-
-
SLC26A4_000157
compound heterozygous, VKGL data sharing initiative Nederland
PubMed: Batissoco 2021
ClinVar-SCV001792214
,
ClinVar-188878
rs542620119
CLASSIFICATION record, Germline
yes
-
-
-
-
VKGL-NL_Nijmegen
,
Karina Lezirovitz Mandelbaum
?/.
1
-
c.562A>G
r.(?)
p.(Ile188Val)
-
VUS
g.107314755A>G
-
-
-
SLC26A4_000263
-
-
-
rs753119943
CLASSIFICATION record
-
-
-
-
-
MobiDetails
+?/+?
1
5
c.563T>C
r.(?)
p.(Ile188Thr)
ACMG
VUS
g.107314756T>C
g.107674311T>C
-
-
SLC26A4_000043
heterozygous; Mutation
PubMed: Huang S 2011
; USMA-
missense variant in MSV3d
-
-
Germline
-
0/400 controls
-
-
-
Anne-Françoise Roux
?/.
1
-
c.572C>T
r.(?)
p.(Ala191Val)
-
VUS
g.107314765C>T
-
-
-
SLC26A4_000243
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/+, +/.
2
5
c.578C>T
r.(?)
p.(Thr193Ile)
-
pathogenic
g.107314771C>T
g.107674326C>T
-
-
SLC26A4_000075
heterozygous; Mutation, not in 0/404 hearing controls
PubMed: V.de Moraes 2013
; USMA-
missense variant in MSV3d
-
rs111033348
Germline
yes
0/60 controls, 1/206 cases (het)
-
-
-
Zippi Brownstein
,
Anne-Françoise Roux
+?/+?
3
5
c.589G>A
r.(?)
p.(Gly197Arg)
ACMG
VUS
g.107314782G>A
g.107674337G>A
-
-
SLC26A4_000050
heterozygous; Mutation
PubMed: Huang S 2011
; USMA-
missense variant in MSV3d
-
rs111033380
Germline
-
0/400 controls
-
-
-
Anne-Françoise Roux
-/., -?/.
2
-
c.601-17C>T
r.(=)
p.(=)
-
benign, likely benign
g.107315373C>T
g.107674928C>T
SLC26A4(NM_000441.2):c.601-17C>T
-
SLC26A4_000158
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
,
VKGL-NL_AMC
-/., -?/.
2
-
c.601-5C>T
r.spl?
p.?
-
benign, likely benign
g.107315385C>T
-
SLC26A4(NM_000441.1):c.601-5C>T, SLC26A4(NM_000441.2):c.601-5C>T
-
SLC26A4_000244
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_AMC
+/+
1
5i
c.601-1G>A
r.spl?
p.?
-
pathogenic
g.107315389G>A
g.107674944G>A
Pathogenic, exon 6 acceptor splice site
-
SLC26A4_000098
heterozygous; Likely pathogenic mutation
PubMed: K.Tsukamoto 2003
-
-
Germline
-
0/192 controls
-
-
-
Anne-Françoise Roux
+/., +?/?
12
6
c.626G>T
r.(?)
p.(Gly209Val)
ACMG
pathogenic, pathogenic (recessive), VUS
g.107315415G>T
g.107674970G>T
-
-
SLC26A4_000082, SLC26A4_000159
heterozygous; possible pathogenic effect discussed in Choi , 2009; Mutation,
2 more items
PubMed: A.Pera 2008
; USMA-
missense variant in MSV3d
,
PubMed: Roman 2020
,
Journal: Roman 2020
,
3 more items
-
rs111033303
CLASSIFICATION record, Germline
-
0/428 controls
-
-
-
Johan den Dunnen
,
VKGL-NL_Nijmegen
,
Anne-Françoise Roux
+/+
1
6
c.662dup
r.(?)
p.(Gly222Trpfs*38)
-
pathogenic
g.107315451dup
g.107675006dup
662_663insG (p.G221)
-
SLC26A4_000062
heterozygous; Pathogenic
PubMed: Jiang H 2012
-
-
Germline
-
-
-
-
-
Anne-Françoise Roux
+?/.
1
-
c.692T>A
r.(?)
p.(Val231Glu)
-
likely pathogenic
g.107315481T>A
-
-
-
SLC26A4_000259
-
-
-
-
CLASSIFICATION record
-
-
-
-
-
MobiDetails
+/.
1
-
c.697G>C
r,(?)
p.(Val233Leu)
-
pathogenic (recessive)
g.107315486G>C
g.107675041G>C
-
-
SLC26A4_000293
combination of alleles not reported
PubMed: Wu 2019
-
-
Germline
-
1/1291 cases hearing loss
-
-
-
Johan den Dunnen
+/., ?/.
2
-
c.706C>G
r,(?), r.(?)
p.(Leu236Val)
-
pathogenic (recessive), VUS
g.107315495C>G
g.107675050C>G
-
-
SLC26A4_000216
combination of alleles not reported, VKGL data sharing initiative Nederland
PubMed: Wu 2019
-
-
CLASSIFICATION record, Germline
-
3/1291 cases hearing loss
-
-
-
Johan den Dunnen
,
VKGL-NL_Nijmegen
+/+, +/.
6
6
c.707T>C
r.(?)
p.(Leu236Pro)
-
pathogenic
g.107315496T>C
g.107675051T>C
Pathogenic, functional studies showed no actvity of mutant pendrin (Scott et al;2000),
1 more item
-
SLC26A4_000085, SLC26A4_000160
heterozygous; loss of function mutation (Scott ,2000); Pathogenic, heterozygous; Mutation,
2 more items
PubMed: B.Choi 2009
; USMA-
missense variant in MSV3d
,
1 more item
-
rs80338848
CLASSIFICATION record, Germline
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_Nijmegen
,
Anne-Françoise Roux
+/., +?/.
31
-
c.716T>A
r.(?)
p.(Val239Asp)
-
likely pathogenic, pathogenic, pathogenic (recessive)
g.107315505T>A
g.107675060T>A
SLC26A4(NM_000441.1):c.716T>A (p.V239D)
-
SLC26A4_000161
9 heterozygous, no homozygous;
Clinindb (India)
, VKGL data sharing initiative Nederland
PubMed: Narang 2020
,
Journal: Narang 2020
,
PubMed: Park 2003
,
PubMed: Naz 2017
,
PubMed: Richard 2019
-
rs111033256
CLASSIFICATION record, Germline
-
9/2794 individuals
-
-
-
Johan den Dunnen
,
VKGL-NL_Rotterdam
,
VKGL-NL_Nijmegen
,
Mohammed Faruq
+/., +?/?
2
6
c.754T>C
r,(?), r.(?)
p.(Ser252Pro)
ACMG
pathogenic (recessive), VUS
g.107315543T>C
g.107675098T>C
-
-
SLC26A4_000053
combination of alleles not reported, heterozygous; Mutation
PubMed: Huang S 2011
; USMA-
missense variant in MSV3d
,
PubMed: Wu 2019
-
-
Germline
-
0/400 controls, 5/1291 cases hearing loss
-
-
-
Johan den Dunnen
,
Anne-Françoise Roux
-/.
1
-
c.766-20A>C
r.(=)
p.(=)
-
benign
g.107323627A>C
-
SLC26A4(NM_000441.2):c.766-20A>C
-
SLC26A4_000240
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
+/+
1
7
c.783dup
r.(?)
p.(Gln262Serfs*5)
-
pathogenic
g.107323664dup
g.107683219dup
783_784insT (X286)
-
SLC26A4_000086
heterozygous; Mutation
PubMed: C.Campbell 2001
-
-
Germline
-
-
-
-
-
Anne-Françoise Roux
+?/?
1
7
c.812A>G
r.(?)
p.(Asp271Gly)
ACMG
VUS
g.107323693A>G
g.107683248A>G
-
-
SLC26A4_000046
heterozygous; Mutation
PubMed: Huang S 2011
; USMA-
missense variant in MSV3d
-
-
Germline
-
0/400 controls
-
-
-
Anne-Françoise Roux
?/.
1
-
c.841G>A
r.(?)
p.(Val281Ile)
-
VUS
g.107323722G>A
g.107683277G>A
SLC26A4(NM_000441.1):c.841G>A (p.V281I)
-
SLC26A4_000217
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+?/., -?/?
2
7
c.845G>A
r.(?)
p.(Cys282Tyr)
-
likely benign, likely pathogenic
g.107323726G>A
g.107683281G>A
-
-
SLC26A4_000137
heterozygous; Reduced function, VKGL data sharing initiative Nederland
de Moraes 2016; USMA-
missense variant in MSV3d
-
rs111033454
CLASSIFICATION record, Germline
-
-
-
-
-
VKGL-NL_Nijmegen
,
Silvia Dossena
-/., -?/., ?/.
3
-
c.849G>C
r.(?)
p.(Met283Ile)
-
benign, likely benign, VUS
g.107323730G>C
g.107683285G>C
SLC26A4(NM_000441.1):c.849G>C (p.M283I), SLC26A4(NM_000441.2):c.849G>C (p.M283I)
-
SLC26A4_000218
VKGL data sharing initiative Nederland
-
-
rs146348818
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_AMC
,
MobiDetails
?/.
1
-
c.850G>A
r.(?)
p.(Ala284Thr)
-
VUS
g.107323731G>A
-
SLC26A4(NM_000441.2):c.850G>A (p.A284T)
-
SLC26A4_000245
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_VUmc
+/+
5
7
c.863dup
r.(?)
p.(Leu288Phefs*3)
-
pathogenic
g.107323744dup
g.107683299dup
863-864insT p.Leu288PhefsX3, 863-864insT, p.Leu288PhefsX3
-
SLC26A4_000011, SLC26A4_000012, SLC26A4_000013
heterozygous; Pathogenic, homozygous; Pathogenic
PubMed: Yazdanpanahil 2013
-
-
Germline
-
0/200 controls
-
-
-
Anne-Françoise Roux
?/.
1
-
c.872G>A
r.(?)
p.(Arg291Gln)
-
VUS
g.107323753G>A
g.107683308G>A
-
-
SLC26A4_000231
2 heterozygous, no homozygous;
Clinindb (India)
PubMed: Narang 2020
,
Journal: Narang 2020
-
rs138816005
Germline
-
2/2795 individuals
-
-
-
Mohammed Faruq
+/+
13
7
c.882_883del
r.(?)
p.(His294Glnfs*35)
-
pathogenic
g.107323763_107323764del
g.107683318_107683319del
881-882delAC, p.His294GlnfsX35
-
SLC26A4_000014, SLC26A4_000015, SLC26A4_000016, SLC26A4_000017, SLC26A4_000018, SLC26A4_000019
heterozygous; Pathogenic, homozygous; Pathogenic, homozygous; Pathologic
PubMed: Yazdanpanahil 2013
-
-
Germline
-
0/200 controls
-
-
-
Anne-Françoise Roux
?/.
1
-
c.893T>G
r.(?)
p.(Val298Gly)
-
VUS
g.107323774T>G
-
SLC26A4(NM_000441.2):c.893T>G (p.V298G)
-
SLC26A4_000266
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
-/., -?/.
2
-
c.898A>C
r.(?)
p.(Ile300Leu)
-
benign, likely benign
g.107323779A>C
g.107683334A>C
SLC26A4(NM_000441.1):c.898A>C (p.I300L)
-
SLC26A4_000165
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_Nijmegen
+/+, +/.
3
7
c.916dup
r,(?), r.(?)
p.(Val306Glyfs*24), p.(Val306GlyfsTer24)
-
pathogenic, pathogenic (recessive)
g.107323797dup
g.107683352dup
916dupG, 916_917insG, 917insG (Frameshift)
-
SLC26A4_000061
combination of alleles not reported, heterozygous; Mutation, no variant 2nd chromosome
PubMed: Huang S 2011
,
PubMed: Wu 2019
-
-
Germline
-
0/400 controls, 1/1291 cases hearing loss, 5/1291 cases hearing loss
-
-
-
Johan den Dunnen
,
Anne-Françoise Roux
+/+
1
7
c.917del
r.(?)
p.(Val306Glyfs*3)
-
pathogenic
g.107323798del
g.107683353del
-
-
SLC26A4_000088
heterozygous; Pathogenic
PubMed: K.Tsukamoto 2003
-
-
Germline
-
0/192 controls
-
-
-
Anne-Françoise Roux
+/.
1
-
c.918+2T>C
r.spl
p.?
-
pathogenic (recessive)
g.107323801T>C
g.107683356T>C
-
-
SLC26A4_000294
combination of alleles not reported
PubMed: Wu 2019
-
-
Germline
-
1/1291 cases hearing loss
-
-
-
Johan den Dunnen
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