Global Variome shared LOVD
RLBP1 (retinaldehyde binding protein 1)
LOVD v.3.0 Build 30b [
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Curator:
Johan den Dunnen
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All variants in the RLBP1 gene
This database is one of the
"Eye disease"
gene variant databases.
The variants shown are described using the NM_000326.4 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.
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
Allele
: On which allele is the variant located? Does not necessarily imply inheritance! 'Paternal' (confirmed or inferred), 'Maternal' (confirmed or inferred), 'Parent #1' or #2 for compound heterozygosity without having screened the parents, 'Unknown' for heterozygosity without having screened the parents, 'Both' for homozygozity.
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
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|
Text
Arg|Ser
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!
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'
!=""
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!=""
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'
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277 entries on 3 pages. Showing entries 1 - 100.
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Effect
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
+?/.
6i_9_
c.(525+1_526-1)_*418{0}5
r.?
p.?
ACMG
likely pathogenic
g.(89755133_89758290)_(89753098_?)del
g.(89211902_89215059)_(89209867_?)del
del ex7-9, (?_526)_(954_?)del
-
RLBP1_000076
-
PubMed: Hitti-Malin 2022
,
Journal: Hitti-Malin 2022
-
-
Germline
-
-
-
-
-
Rebekkah Hitti-Malin
+?/.
-
c.(526+1_527-1)_(954+?)del
r.?
p.(Ile176Argfs*36)
-
likely pathogenic
g.?
-
c.(526+1_527-1)_(954+?)del
-
IGF1R_000000
-
PubMed: Panneman 2023
-
-
Unknown
-
-
-
-
-
Daan Panneman
?/.
-
c.-70G>A
r.(?)
p.(?)
-
VUS
g.89762276C>T
g.89219045C>T
RLBP1 c.-70 G > A, p.(?), rs3743384
-
RLBP1_000066
heterozygous
PubMed: Donato-2021
-
rs3743384
Germline
yes
-
-
-
-
LOVD
?/.
-
c.-70G>A
r.(?)
p.(?)
-
VUS
g.89762276C>T
g.89219045C>T
RLBP1 c.-70 G > A, p.(?), rs3743384
-
RLBP1_000066
heterozygous
PubMed: Donato-2021
-
rs3743384
Germline
yes
-
-
-
-
LOVD
+/.
6i_9i
c.?
r.?
p.?
-
pathogenic (recessive)
g.?
-
del ex7-9
-
IGF1R_000000
-
PubMed: Bocquet 2013
-
-
Germline
-
-
-
-
-
Johan den Dunnen
-?/.
4
c.?
r.?
p.?
-
likely benign
g.?
-
c.40C>T
-
IGF1R_000000
-
PubMed: Golovleva-2010
-
-
Germline
-
-
-
-
-
LOVD
-?/.
4
c.?
r.?
p.?
-
likely benign
g.?
-
c.40C>T
-
IGF1R_000000
-
PubMed: Golovleva-2010
-
-
Germline
-
6/143 healthy blood donors
-
-
-
LOVD
+?/.
-
c.?
r.0?
p.0?
-
likely pathogenic
g.89750128_89757489del
-
chr15:g.89750128_89757489del
-
IGF1R_000000
heterozygous
PubMed: Turro 2020
-
-
Germline/De novo (untested)
?
-
-
-
-
LOVD
+?/.
-
c.?
r.0?
p.0?
-
likely pathogenic
g.89750128_89757489del
-
chr15:g.89750128_89757489del
-
IGF1R_000000
homozygous
PubMed: Turro 2020
-
-
Germline/De novo (untested)
?
-
-
-
-
LOVD
+?/.
-
c.?
r.(?)
p.(?)
-
likely pathogenic
g.?
g.?
7.36-kb homozygous deletion encompassing the last 3 exons of RLBP1 (7, 8, and 9) and part of the intergenic region between RLBP1 and ABHD2
-
IGF1R_000000
homozygous
PubMed: Humbert 2006
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
-
c.?
r.(?)
p.(?)
-
likely pathogenic
g.?
g.?
Exons7_9del/Exons7_9del
-
IGF1R_000000
deletion of exons 7 through 9; homozygous
PubMed: Dessalces 2013
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
-
c.?
r.(?)
p.(?)
-
likely pathogenic
g.?
g.?
Exons7_9del/Exons7_9del
-
IGF1R_000000
deletion of exons 7 through 9; homozygous
PubMed: Dessalces 2013
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
-
c.?
r.(?)
p.(?)
-
likely pathogenic
g.?
g.?
Exons7_9del/Exons7_9del
-
IGF1R_000000
deletion of exons 7 through 9; homozygous
PubMed: Dessalces 2013
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
-
c.?
r.(?)
p.(?)
-
likely pathogenic
g.?
g.?
Exons7_9del/Exons7_9del
-
IGF1R_000000
deletion of exons 7 through 9; homozygous
PubMed: Dessalces 2013
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
-
c.?
r.(?)
p.(?)
-
likely pathogenic
g.?
g.?
Exons7_9del/Exons7_9del
-
IGF1R_000000
deletion of exons 7 through 9; homozygous
PubMed: Dessalces 2013
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
-
c.?
r.(?)
p.(?)
-
likely pathogenic
g.?
g.?
Exons7_9del/Exons7_9del
-
IGF1R_000000
deletion of exons 7 through 9; homozygous
PubMed: Dessalces 2013
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
-
c.?
r.(?)
p.(?)
-
likely pathogenic
g.?
g.?
Exons7_9del/Exons7_9del
-
IGF1R_000000
deletion of exons 7 through 9; homozygous
PubMed: Dessalces 2013
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
-
c.?
r.(?)
p.(?)
-
likely pathogenic
g.?
g.?
Exons7_9del/Exons7_9del
-
IGF1R_000000
deletion of exons 7 through 9; homozygous
PubMed: Dessalces 2013
-
-
Germline
yes
-
-
-
-
LOVD
+/.
3i
c.13-2_13-1delinsCC
r.spl?
p.?
-
pathogenic (recessive)
g.89761925_89761926delinsGG
-
c.(13-2)_(13-1)delinsCC
-
RLBP1_000069
-
PubMed: Colombo-2020
-
-
Germline
-
-
-
-
-
LOVD
+?/.
-
c.13-1G>C
r.spl
p.?
ACMG
likely pathogenic
g.89761925C>G
g.89218694C>G
RLBP1 c.13-1G>C, p.?
-
RLBP1_000079
compound heterozygous, probably causal
PubMed: Zhu 2022
-
-
Germline/De novo (untested)
?
-
-
-
-
LOVD
+?/.
-
c.25C>T
r.(?)
p.(Arg9Cys)
-
likely pathogenic
g.89761912G>A
g.89218681G>A
-
-
RLBP1_000044
-
PubMed: Stone 2017
-
-
Germline
-
-
-
-
-
LOVD
+?/.
-
c.25C>T
r.(?)
p.(Arg9Cys)
-
likely pathogenic
g.89761912G>A
g.89218681G>A
p.R9C/p.Y111stop
-
RLBP1_000044
heterozygous
PubMed: Dessalces 2013
-
-
Germline
yes
0/112 alleles
-
-
-
LOVD
+/.
-
c.25C>T
r.(?)
p.(Arg9Cys)
-
pathogenic
g.89761912G>A
g.89218681G>A
RLBP1 c.25C T:pArg9Cys
-
RLBP1_000044
heterozygous
PubMed: Lima-de-Carvalho 2020
-
-
Germline
yes
-
-
-
-
LOVD
+/.
-
c.25C>T
r.(?)
p.(Arg9Cys)
-
pathogenic
g.89761912G>A
g.89218681G>A
RLBP1 c.25C T:pArg9Cys
-
RLBP1_000044
heterozygous
PubMed: Lima-de-Carvalho 2020
-
-
Germline
yes
-
-
-
-
LOVD
+/.
4
c.34_44del
r.(?)
p.(Pro12Thrfs*36)
ACMG
pathogenic
g.89761894_89761904del
g.89218663_89218673del
NM_000326.4:c.34_44del, NP_000317.1:p.(Pro12ThrfsTer36), NC_000015.9:g.89761894_89761904del
-
RLBP1_000056
-
PubMed: Wang 2018
-
-
Germline
?
-
-
-
-
LOVD
+?/.
4
c.34_44del
r.(?)
p.(Pro12Thrfs*36)
-
likely pathogenic (recessive)
g.89761893_89761903del
-
c.34_44del11bp
-
RLBP1_000056
-
PubMed: Liu-2020
-
-
Germline
-
-
-
-
-
LOVD
?/.
-
c.40G>C
r.(?)
p.(Glu14Gln)
ACMG
VUS
g.89761897C>G
g.89218666C>G
-
-
RLBP1_000083
ACMG PM2; no variant 2nd chromosome
PubMed: Weisschuh 2024
-
-
Germline
-
-
-
-
-
Johan den Dunnen
?/.
-
c.42G>T
r.(?)
p.(Glu14Asp)
-
VUS
g.89761895C>A
g.89218664C>A
-
-
RLBP1_000021
-
PubMed: Koyanagi 2019
,
Journal: Koyanagi 2019
-
-
Germline
-
2/1204 cases with retinitis pigmentosa
-
-
-
Yoshito Koyanagi
?/.
-
c.55C>T
r.(?)
p.(Arg19Cys)
-
VUS
g.89761882G>A
g.89218651G>A
-
-
RLBP1_000020
-
PubMed: Koyanagi 2019
,
Journal: Koyanagi 2019
-
rs369127471
Germline
-
1/1204 cases with retinitis pigmentosa
-
-
-
Yoshito Koyanagi
?/.
-
c.55C>T
r.(?)
p.(Arg19Cys)
ACMG
VUS
g.89761882G>A
g.89218651G>A
RLBP1 c.55C>T(;)282del, V1: c.55C>T, (p.Arg19Cys)
-
RLBP1_000020
alleles in cis or trans; heterozygous
PubMed: Chen 2021
-
-
Unknown
?
-
-
-
-
LOVD
?/.
-
c.55C>T
r.(?)
p.(Arg19Cys)
-
VUS
g.89761882G>A
g.89218651G>A
RLBP1 c.55C>T(;)282del; p.(Arg19Cys)
-
RLBP1_000020
heterozygous
PubMed: Chen 2021
-
-
Germline/De novo (untested)
?
Taiwan Biobank: 0; GnomAD_exome_East: 0; GnomAD_All: 0.00000796
-
-
-
LOVD
-?/.
-
c.57T>C
r.(?)
p.(Arg19=)
-
likely benign
g.89761880A>G
g.89218649A>G
RLBP1(NM_000326.4):c.57T>C (p.R19=)
-
RLBP1_000011
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+/.
-
c.79del
r.(?)
p.(Thr27Profs*26)
ACMG
pathogenic (recessive)
g.89761858del
g.89218627del
79delA
-
RLBP1_000036
ACMG PVS1, PM2, PP1
PubMed: Al-Bdour 2020
-
rs1567124404
Germline
yes
-
-
-
-
Johan den Dunnen
?/.
-
c.124C>T
r.(?)
p.(Arg42Cys)
-
VUS
g.89761813G>A
g.89218582G>A
RLBP1(NM_000326.4):c.124C>T (p.R42C)
-
RLBP1_000033
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
-?/.
-
c.126C>T
r.(?)
p.(Arg42=)
-
likely benign
g.89761811G>A
g.89218580G>A
RLBP1(NM_000326.4):c.126C>T (p.R42=), RLBP1(NM_000326.5):c.126C>T (p.R42=)
-
RLBP1_000010
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
-/.
-
c.126C>T
r.(?)
p.(Arg42=)
-
benign
g.89761811G>A
g.89218580G>A
RLBP1(NM_000326.4):c.126C>T (p.R42=), RLBP1(NM_000326.5):c.126C>T (p.R42=)
-
RLBP1_000010
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; homozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; heterozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; heterozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; heterozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; heterozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; heterozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; heterozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4
c.141G>A
r.(?)
p.[Lys47=;?]
-
likely pathogenic
g.89761796C>T
g.89218565C>T
324G>A
-
RLBP1_000074
annotation obsolete, this change is probably c.141G>A; silent mutation with a strong suspiction of splicing alteration; heterozygous
PubMed: Eichers 2002
-
rs766278489
Germline
yes
-
-
-
-
LOVD
+?/.
4i
c.141+2T>C
r.spl
p.(?)
-
likely pathogenic
g.89761794A>G
g.89218563A>G
1335T>C, IVS3+2 (GT to GC)
-
RLBP1_000073
annotation obsolete, this change is probably c.141+2T>C, transcript used not indicated but was probably different without exon 1 that is present in NM_000326.4
PubMed: Morimura 1999
-
-
Germline
yes
0/69 controls
-
-
-
LOVD
+?/.
4i
c.141+2T>C
r.spl
p.(?)
-
likely pathogenic
g.89761794A>G
g.89218563A>G
IVS3+2 T>C
-
RLBP1_000073
annotation obsolete, this change is probably c.141+2T>C, transcript used not indicated but was probably different without exon 1 that is present in NM_000326.4; heterozygous
PubMed: Eichers 2002
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
4i
c.141+2T>C
r.spl
p.(?)
-
likely pathogenic
g.89761794A>G
g.89218563A>G
IVS3+2 T>C
-
RLBP1_000073
annotation obsolete, this change is probably c.141+2T>C, transcript used not indicated but was probably different without exon 1 that is present in NM_000326.4; heterozygous
PubMed: Eichers 2002
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
4i
c.141+2T>C
r.spl
p.(?)
-
likely pathogenic
g.89761794A>G
g.89218563A>G
IVS3+2 T>C
-
RLBP1_000073
annotation obsolete, this change is probably c.141+2T>C, transcript used not indicated but was probably different without exon 1 that is present in NM_000326.4; homozygous
PubMed: Eichers 2002
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
4i
c.141+2T>C
r.spl
p.(?)
-
likely pathogenic
g.89761794A>G
g.89218563A>G
IVS3+2 T>C
-
RLBP1_000073
annotation obsolete, this change is probably c.141+2T>C, transcript used not indicated but was probably different without exon 1 that is present in NM_000326.4; heterozygous
PubMed: Eichers 2002
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
4i
c.141+2T>C
r.spl
p.(?)
-
likely pathogenic
g.89761794A>G
g.89218563A>G
IVS3+2 T>C
-
RLBP1_000073
annotation obsolete, this change is probably c.141+2T>C, transcript used not indicated but was probably different without exon 1 that is present in NM_000326.4; heterozygous
PubMed: Eichers 2002
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
4i
c.141+2T>C
r.spl
p.(?)
-
likely pathogenic
g.89761794A>G
g.89218563A>G
IVS3+2 T>C
-
RLBP1_000073
annotation obsolete, this change is probably c.141+2T>C, transcript used not indicated but was probably different without exon 1 that is present in NM_000326.4; heterozygous
PubMed: Eichers 2002
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
4i
c.141+2T>C
r.spl
p.(?)
-
likely pathogenic
g.89761794A>G
g.89218563A>G
IVS3+2 T>C
-
RLBP1_000073
annotation obsolete, this change is probably c.141+2T>C, transcript used not indicated but was probably different without exon 1 that is present in NM_000326.4; heterozygous
PubMed: Eichers 2002
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
4i
c.141+2T>C
r.spl
p.(?)
-
likely pathogenic
g.89761794A>G
g.89218563A>G
IVS3+2 T>C
-
RLBP1_000073
annotation obsolete, this change is probably c.141+2T>C, transcript used not indicated but was probably different without exon 1 that is present in NM_000326.4; heterozygous
PubMed: Eichers 2002
-
-
Germline
yes
-
-
-
-
LOVD
-/.
-
c.141+6G>A
r.(=)
p.(=)
-
benign
g.89761790C>T
g.89218559C>T
RLBP1(NM_000326.4):c.141+6G>A, RLBP1(NM_000326.5):c.141+6G>A
-
RLBP1_000032
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
-?/.
-
c.141+6G>A
r.(=)
p.(=)
-
likely benign
g.89761790C>T
g.89218559C>T
RLBP1(NM_000326.4):c.141+6G>A, RLBP1(NM_000326.5):c.141+6G>A
-
RLBP1_000032
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+?/.
4i
c.142-1G>A
r.spl?
p.?
-
likely pathogenic
g.89760556C>T
-
c.142-1G>A, splice defect
-
RLBP1_000052
-
PubMed: Littink-2012
-
-
Germline
-
-
-
-
-
LOVD
+?/.
4i
c.142-1G>A
r.spl?
p.?
-
likely pathogenic
g.89760556C>T
-
c.142-1G>A, splice defect
-
RLBP1_000052
-
PubMed: Littink-2012
-
-
Germline
-
-
-
-
-
LOVD
-/.
-
c.191G>A
r.(?)
p.(Arg64Gln)
-
benign
g.89760506C>T
g.89217275C>T
-
-
RLBP1_000019
-
PubMed: Koyanagi 2019
,
Journal: Koyanagi 2019
-
rs201865787
Germline
-
46/1204 cases with retinitis pigmentosa
-
-
-
Yoshito Koyanagi
-/.
-
c.191G>A
r.(?)
p.(Arg64Gln)
-
benign
g.89760506C>T
g.89217275C>T
RLBP1(NM_000326.4):c.191G>A (p.R64Q)
-
RLBP1_000019
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
?/.
-
c.191G>A
r.(?)
p.(Arg64Gln)
-
VUS
g.89760506C>T
g.89217275C>T
-
-
RLBP1_000019
-
PubMed: Xu 2014
-
rs201865787
Germline
-
3/314 case chromosomes
-
-
-
LOVD
?/.
-
c.191G>A
r.(?)
p.(Arg64Gln)
-
VUS
g.89760506C>T
g.89217275C>T
-
-
RLBP1_000019
-
PubMed: Xu 2014
-
-
Germline
-
3/314 case chromosomes
-
-
-
LOVD
?/.
-
c.191G>A
r.(?)
p.(Arg64Gln)
-
VUS
g.89760506C>T
g.89217275C>T
-
-
RLBP1_000019
-
PubMed: Xu 2014
-
-
Germline
-
3/314 case chromosomes
-
-
-
LOVD
+?/.
-
c.203del
r.(?)
p.(Glu68Glyfs*51)
-
likely pathogenic
g.89760494del
g.89217263del
RLBP1, variant 1: c.203del/p.E68Gfs*51, variant 2: c.203del/p.E68Gfs*51
-
RLBP1_000065
solved, homozygous
PubMed: Weisschuh 2020
-
-
Unknown
?
-
-
-
-
LOVD
+?/.
-
c.203del
r.(?)
p.(Glu68Glyfs*51)
-
likely pathogenic
g.89760494del
g.89217263del
RLBP1 c.203del, p.(Glu68Glyfs*51)
-
RLBP1_000065
homozygous
PubMed: Hipp 2015
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
5
c.214G>C
r.(?)
p.(Ala72Pro)
-
likely pathogenic
g.89760483C>G
-
c.214G>C
-
RLBP1_000051
-
PubMed: Collin-2011
-
-
Germline
-
0/360 controls
-
-
-
LOVD
?/.
-
c.221C>T
r.(?)
p.(Ala74Val)
-
VUS
g.89760476G>A
g.89217245G>A
-
-
RLBP1_000018
-
PubMed: Koyanagi 2019
,
Journal: Koyanagi 2019
-
-
Germline
-
1/1204 cases with retinitis pigmentosa
-
-
-
Yoshito Koyanagi
?/.
-
c.229G>C
r.(?)
p.(Gly77Arg)
-
VUS
g.89760468C>G
g.89217237C>G
-
-
RLBP1_000017
-
PubMed: Koyanagi 2019
,
Journal: Koyanagi 2019
-
rs755885208
Germline
-
1/1204 cases with retinitis pigmentosa
-
-
-
Yoshito Koyanagi
-?/.
-
c.231G>A
r.(?)
p.(Gly77=)
-
likely benign
g.89760466C>T
g.89217235C>T
RLBP1(NM_000326.4):c.231G>A (p.G77=)
-
RLBP1_000035
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
?/.
-
c.241G>A
r.(?)
p.(Ala81Thr)
ACMG
VUS
g.89760456C>T
g.89217225C>T
-
-
RLBP1_000082
ACMG PM2
PubMed: Weisschuh 2024
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+?/.
5
c.254C>T
r.(?)
p.(Ala85Val)
-
likely pathogenic
g.89760443G>A
-
c.254C>T
-
RLBP1_000057
-
PubMed: Eisenberger-2013
-
-
Germline
-
-
-
-
-
LOVD
+?/.
-
c.255_258dup
r.(?)
p.(Arg87Glyfs*27)
-
likely pathogenic
g.89760439_89760442dup
g.89217208_89217211dup
RLBP1, variant 1: c.255_258dup/p.R87Gfs*27, variant 2: c.255_258dup/p.R87Gfs*27
-
RLBP1_000064
solved, homozygous
PubMed: Weisschuh 2020
-
-
Unknown
?
-
-
-
-
LOVD
+/.
-
c.255_258dup
r.(?)
p.(Arg87GlyfsTer27)
ACMG
pathogenic (recessive)
g.89760439_89760442dup
g.89217208_89217211dup
-
-
RLBP1_000064
ACMG PM2, PVS1, PP5
PubMed: Weisschuh 2024
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+?/.
-
c.282del
r.(?)
p.(Phe95SerfsTer24)
-
likely pathogenic
g.89760415del
g.89217184del
282delC
-
RLBP1_000012
-
PubMed: Huang 2015
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
-
c.282del
r.(?)
p.(Phe95SerfsTer24)
-
likely pathogenic
g.89760415del
g.89217184del
282delC
-
RLBP1_000012
-
PubMed: Huang 2015
-
-
Germline
yes
-
-
-
-
LOVD
+?/.
5
c.282del
r.(?)
p.(Phe95Serfs*24)
-
likely pathogenic
g.89760415del
g.89217184del
RLBP1:NM_000326:exon5:c.282delC:p.G94fs
-
RLBP1_000012
compound heterozygous
PubMed: Chen 2020
-
-
Germline
?
-
-
-
-
LOVD
+/.
-
c.282del
r.(?)
p.(Phe95Serfs*24)
ACMG
pathogenic
g.89760415del
g.89217184del
RLBP1 c.[282del];[282del], V1: c.282delC, (p.Phe95SerfsTer24)
-
RLBP1_000012
homozygous
PubMed: Chen 2021
-
-
Unknown
?
-
-
-
-
LOVD
+/.
-
c.282del
r.(?)
p.(Phe95Serfs*24)
ACMG
pathogenic
g.89760415del
g.89217184del
RLBP1 c.[282del];[282del], V1: c.282delC, (p.Phe95SerfsTer24)
-
RLBP1_000012
alleles in trans; heterozygous
PubMed: Chen 2021
-
-
Unknown
?
-
-
-
-
LOVD
+/.
-
c.282del
r.(?)
p.(Phe95Serfs*24)
ACMG
pathogenic
g.89760415del
g.89217184del
RLBP1 c.55C>T(;)282del, V2: c.282delC, (p.Phe95SerfsTer24)
-
RLBP1_000012
alleles in cis or trans; heterozygous
PubMed: Chen 2021
-
-
Unknown
?
-
-
-
-
LOVD
+/.
-
c.282delC
r.(?)
p.(Phe95SerfsTer24)
-
pathogenic
g.89760415del
g.89217184del
RLBP1 c.55C>T(;)282del; p.(Phe95SerfsTer24)
-
RLBP1_000012
heterozygous
PubMed: Chen 2021
-
-
Germline/De novo (untested)
?
Taiwan Biobank: 0.000989; GnomAD_exome_East: 0.00125; GnomAD_All: 0.0000916
-
-
-
LOVD
+/.
-
c.282delC
r.(?)
p.(Phe95SerfsTer24)
-
pathogenic
g.89760415del
g.89217184del
RLBP1 c.[282del];[282del]; p.(Phe95SerfsTer24)
-
RLBP1_000012
homozygous
PubMed: Chen 2021
-
-
Germline
yes
Taiwan Biobank: 0..000989; GnomAD_exome_East: 0.00125; GnomAD_All: 0.0000916
-
-
-
LOVD
+/.
-
c.282delC
r.(?)
p.(Phe95SerfsTer24)
-
pathogenic
g.89760415del
g.89217184del
RLBP1 c.[282del];[282del]; p.(Phe95SerfsTer24)
-
RLBP1_000012
homozygous
PubMed: Chen 2021
-
-
Germline
yes
Taiwan Biobank: 0..000989; GnomAD_exome_East: 0.00125; GnomAD_All: 0.0000916
-
-
-
LOVD
+?/.
-
c.286_297del
r.(?)
p.(Phe96_Phe99del)
-
likely pathogenic
g.89760405_89760416del
g.89217174_89217185del
RLBP1(NM_000326.5):c.286_297delTTCCTGCGCTTC (p.F96_F99del)
-
RLBP1_000009
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
+/.
5
c.286_297del
r.(?)
p.(Phe96_Phe99del)
-
pathogenic
g.89760388_89760399del
-
-
-
RLBP1_000009
Variant Error [EMISMATCH]: This variant seems to mismatch; the genomic and the transcript variant seems to not belong together. Please fix this entry and then remove this message.
Sharon, submitted
-
-
Germline
-
-
-
-
-
Dror Sharon
+/.
-
c.286_297del
r.(?)
p.(Phe96_Phe99del)
ACMG
pathogenic
g.89760400_89760411del
-
-
-
RLBP1_000009
-
PubMed: Sharon 2019
-
-
Germline
-
2/2420 IRD families
-
-
-
Global Variome, with Curator vacancy
+?/.
-
c.286_297del
r.(?)
p.(Phe96_Phe99del)
-
likely pathogenic
g.89760405_89760416del
g.89217174_89217185del
-
-
RLBP1_000009
-
PubMed: Patel 2016
-
-
Germline
-
-
-
-
-
LOVD
+/.
-
c.286_297del
r.(?)
p.(Phe96_Phe99del)
-
pathogenic
g.89760405_89760416del
g.89217174_89217185del
RLBP1 c.286_297:p.Phe96_99 deletion
-
RLBP1_000009
heterozygous
PubMed: Lima-de-Carvalho 2020
-
-
Germline
yes
-
-
-
-
LOVD
+/.
-
c.286_297del
r.(?)
p.(Phe96_Phe99del)
-
pathogenic
g.89760405_89760416del
g.89217174_89217185del
RLBP1 c.286_297:p.Phe96_99 deletion
-
RLBP1_000009
heterozygous
PubMed: Lima-de-Carvalho 2020
-
-
Germline
yes
-
-
-
-
LOVD
-?/.
-
c.303C>T
r.(?)
p.(Arg101=)
-
likely benign
g.89760394G>A
-
RLBP1(NM_000326.4):c.303C>T (p.R101=)
-
RLBP1_000042
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
-?/.
-
c.306A>C
r.(?)
p.(Ala102=)
-
likely benign
g.89760391T>G
g.89217160T>G
RLBP1(NM_000326.4):c.306A>C (p.A102=), RLBP1(NM_000326.5):c.306A>C (p.A102=)
-
RLBP1_000031
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
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