Malaysian Node of the Human Variome Project Database
LDLR (low density lipoprotein receptor)
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Unique variants in the LDLR gene
The variants shown are described using the NM_000527.4 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.
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.
Published as
: Variant as originally reported (e.g. 521delT); listed only when different from "DNA change". Variants seen in animal models, tested in vitro, predicted from RNA analysis, etc. are described between brackets like c.(456C>G).
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
GVS function
: The functional annotation of this position from the Genome Variation Server.
All options:
intergenic
near-gene-5
utr-5
start-lost
coding
non-coding-exon
coding-near-splice
non-coding-exon-near-splice
coding-synonymous
coding-synonymous-near-splice
codingComplex
codingComplex-near-splice
frameshift
frameshift-near-splice
missense
missense-near-splice
splice-5
splice
non-coding-intron-near-splice
intron
splice-3
stop-gained
stop-gained-near-splice
stop-lost
stop-lost-near-splice
utr-3
near-gene-3
Clinical classification
: Clinical classification of variant
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
Published as
: Variant as originally reported (e.g. 521delT); listed only when different from "DNA change". Variants seen in animal models, tested in vitro, predicted from RNA analysis, etc. are described between brackets like c.(456C>G).
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.
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).
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.
60 entries on 1 page. Showing entries 1 - 60.
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Legend
How to query
Effect
Reported
Exon
DNA change (cDNA)
Published as
RNA change
Protein
GVS function
Clinical classification
DNA change (genomic) (hg38)
Published as
Reference
DB-ID
dbSNP ID
Frequency
Variant remarks
Owner
+/.
1
-
c.-152C>T
-
r.(=)
p.(=)
-
-
g.11089397C>T
CT at −152
K L Khoo et al. (2000)
,
ClinVar
LDLR_000037
-
1/9
-
Nuur Athirah Binti Mohd Daud
+/.
1
2
c.77_78del
-
r.(?)
p.(Arg26Metfs*25)
-
ClinVar
g.11100232_11100233del
GA deleted at 77
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
LDLR_000038
rs879254400
1/9
-
Nuur Athirah Binti Mohd Daud
+/., -/.
2
2
c.81C>T
p.Cys27Cys
r.(=)
p.(=)
-
Benign,
ClinVar
g.11100236C>T
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000002
rs2228671
1/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
./.
1
2i
c.190+4A>T
-
r.spl?
p.?
-
ClinVar
g.11100349A>T
-
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000023
rs769446356
1/147
-
Nuur Athirah Binti Mohd Daud
./.
1
2i
c.190+56G>A
-
r.(=)
p.(=)
-
ClinVar
g.11100401G>A
-
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000003
rs3745677
3/147
-
Nuur Athirah Binti Mohd Daud
+/.
2
2i
c.190+58C>T
-
r.(=)
p.(=)
-
-
g.11100403C>T
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
LDLR_000004
rs3745678
7/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/.
2
3
c.268G>A
-
r.(?)
p.(Asp90Asn)
-
ClinVar
g.11102741G>A
D69N, GAT>AAT at 268
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
,
M Azian et ai. (2006)
,
dbSNP
,
ClinVar
LDLR_000039
rs749038326
1/33, 1/9
-
Nuur Athirah Binti Mohd Daud
-?/.
1
3
c.300C>T
-
r.(=)
p.(=)
-
ClinVar
g.11102773C>T
-
Alyaa Al-Khateeb et al. (2011)
dbSNP
LDLR_000005
rs766709484
1/147
-
Nuur Athirah Binti Mohd Daud
+/., ./.
3
3
c.301G>A
-
r.(?)
p.(Glu101Lys)
-
Pathogenic/Likely pathogenic,
ClinVar
g.11102774G>A
p.Glu101Lys in exon 3
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
,
1 more item
LDLR_000024
rs144172724
11/147, 3/10
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/.
2
3i
c.313+1G>A
-
r.spl?
p.?
-
-
g.11102787G>A
G>A at 313+1
(OMIM 0054)
,
ClinVar
,
K L Khoo et al. (2000)
,
ClinVar
,
(OMIM 0054)
LDLR_000031
-
1/10, 1/40
-
Nuur Athirah Binti Mohd Daud
+/.
1
4
c.344G>A
-
r.(?)
p.(Arg115His)
-
ClinVar
g.11105250G>A
CGC>CAC at 344
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
LDLR_000040
rs201102461
2/9
-
Nuur Athirah Binti Mohd Daud
+/., +?/.
2
4
c.415G>C
-
r.(?)
p.(Asp139His)
-
Likely pathogenic,
ClinVar
g.11105321G>C
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000025
rs879254517
1/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/.
1
4
c.530C>T
-
r.(?)
p.(Ser177Leu)
-
Pathogenic/Likely pathogenic
g.11105436C>T
-
Noor Shafina Mohd Nor et al.(2019)
LDLR_000060
rs121908026
-
-
Nur Aisyah Athirah
+/., +?/.
2
4
c.601G>A
-
r.(?)
p.(Glu201Lys)
-
Likely pathogenic,
ClinVar
g.11105507G>A
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000026
rs879254589
9/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/.
1
4
c.660delC
-
r.(?)
p.(Asp221Thrfs*44)
-
-
g.11105566delC
c.660delC in exon 4
Kah Lin Khoo et al. (2016)
LDLR_000053
-
1/10
-
Nuur Athirah Binti Mohd Daud
+/.
2
5
c.757C>T
-
r.(?)
p.(Arg253Trp)
-
-
g.11106627C>T
CGG>TGG at 757
K L Khoo et al. (2000)
,
ClinVar
LDLR_000041
-
1/10, 1/9
-
Nuur Athirah Binti Mohd Daud
+/., +?/.
6
5
c.763T>A
-
r.(?)
p.(Cys255Ser)
-
Likely pathogenic,
ClinVar
g.11106633T>A
C234S, Cys255Ser in exon 5
dbSNP
,
ClinVar
, {DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
3 more items
LDLR_000027
rs879254668
1/10, 10/147, 2/33, 4/40, 7/33
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/.
1
6
c.829G>A
-
r.(?)
p.(Glu277Lys)
-
-
g.11107403G>A
GAG>AAG at 829
K L Khoo et al. (2000)
,
ClinVar
LDLR_000001
-
1
-
Nuur Athirah Binti Mohd Daud
+/., ./.
3
6
c.910G>A
-
r.(?)
p.(Asp304Asn)
-
Pathogenic/Likely pathogenic,
ClinVar
g.11107484G>A
Asp304Asn in exon 6
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
2 more items
LDLR_000006
rs121908030
1/10, 7/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/., -/.
2
6i
c.940+36G>A
-
r.(=)
p.(=)
-
Benign,
ClinVar
g.11107550G>A
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000007
rs13306513
3/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/.
1
6i
c.940+775G>A
-
r.(=)
p.(=)
-
-
g.11108289G>A
-
Say-Hean Lye et al. (2013)
,
dbSNP
LDLR_000036
rs2569556
1
-
Nuur Athirah Binti Mohd Daud
+?/.
1
6i
c.940+1187G>T
-
r.(=)
p.(=)
-
-
g.11108701G>T
-
Livy Alex et al. (2012)
,
dbSNP
LDLR_000035
rs61318752
1/2
-
Nuur Athirah Binti Mohd Daud
+/.
1
7
c.986G>A
-
r.(?)
p.(Cys329Tyr)
-
ClinVar
g.11110697G>A
TGC>TAC at 986
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
LDLR_000045
rs761954844
2/10
-
Nuur Athirah Binti Mohd Daud
+/.
1
7i
c.1060+7C>A
-
r.(=)
p.(=)
-
-
g.11110778C>A
c.1060+7T>C
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
LDLR_000008
rs2738442
18/147
-
Nuur Athirah Binti Mohd Daud
+/.
1
7i
c.1060+7C>T
c.1060+7T>C
r.(=)
p.(=)
-
Uncertain significance
g.11110778C>T
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18}
LDLR_000059
rs2738442
-
-
Nur Aisyah Athirah
+/.
1
7i
c.1060+10G>C
-
r.(=)
p.(=)
-
-
g.11110781G>C
-
Alyaa Al-Khateeb et al. (2011)
,
ClinVar
LDLR_000009
-
5/147
-
Nuur Athirah Binti Mohd Daud
+/.
2
8
c.1132C>T
-
r.(?)
p.(Gln378*)
-
ClinVar
g.11111585C>T
CAG>TAG at 1132
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
LDLR_000046
rs879254802
1, 1/10
-
Nuur Athirah Binti Mohd Daud
-?/.
1
8i
c.1186+41T>A
-
r.(=)
p.(=)
-
ClinVar
g.11111680T>A
-
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000010
rs536387604
1/147
-
Nuur Athirah Binti Mohd Daud
+/., ./.
2
9
c.1194C>T
p.Ile398Ile
r.(=)
p.(=)
-
Conflicting interpretations of pathogenicity,
ClinVar
g.11113285C>T
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000011
rs13306498
5/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/.
2
9
c.1216C>T
-
r.(?)
p.(Arg406Trp)
-
-
g.11113307C>T
R385W
ClinVar
,
M Azian et al. (2006)
,
ClinVar
LDLR_000032
-
1/40, 2/33
-
Nuur Athirah Binti Mohd Daud
+/.
2
9
c.1241T>G
-
r.(?)
p.(Leu414Arg)
-
ClinVar
g.11113332T>G
CTG>CGG at 1242, p.Leu414Arg in exon 9
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
,
Kah Lin Khoo et al. (2016)
,
dbSNP
,
ClinVar
LDLR_000047
rs748554592
1/5, 2/10
-
Nuur Athirah Binti Mohd Daud
+/.
1
9
c.1268T>C
-
r.(?)
p.(Ile423Thr)
-
ClinVar
g.11113359T>C
ATC>ACC at 1269
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
LDLR_000042
rs879254849
1/9
-
Nuur Athirah Binti Mohd Daud
./.
1
9
c.1284C>G
-
r.(?)
p.(Asn428Lys)
-
ClinVar
g.11113375C>G
AAC>AAG at 1283
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
LDLR_000051
rs368708058
1
-
Nuur Athirah Binti Mohd Daud
-/.
1
9i
c.1359-30C>T
-
r.(=)
p.(=)
-
ClinVar
g.11113505C>T
-
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000012
rs1003723
2/147
-
Nuur Athirah Binti Mohd Daud
-?/.
1
10
c.1411A>G
-
r.(?)
p.(Arg471Gly)
-
ClinVar
g.11113587A>G
-
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000013
rs879254891
17/147
-
Nuur Athirah Binti Mohd Daud
-/.
2
10
c.1413A>G
-
r.(=)
p.(=)
-
ClinVar
g.11113589A>G
c.1413G>A, R450R
dbSNP
,
ClinVar
,
M Azian et al. (2006)
,
dbSNP
,
ClinVar
LDLR_000033
rs5930
15/40, 4/33
-
Nuur Athirah Binti Mohd Daud
+/.
1
10
c.1432G>A
-
r.(?)
p.(Gly478Arg)
-
-
g.11113608G>A
GGG>AGG at 1432
K L Khoo et al. (2000)
,
ClinVar
LDLR_000048
-
1/10
-
Nuur Athirah Binti Mohd Daud
+/.
1
10
c.1474G>A
-
r.(?)
p.(Asp492Asn)
-
-
g.11113650G>A
GAC>AAC at 1474
K L Khoo et al. (2000)
,
ClinVar
LDLR_000049
-
1/10
-
Nuur Athirah Binti Mohd Daud
./.
1
10i
c.1586+5G>C
-
r.spl?
p.?
-
ClinVar
g.11113767G>C
c.1586+5 G to C in intron 10
Kah Lin Khoo et al. (2016)
,
dbSNP
,
ClinVar
LDLR_000055
rs781362878
1/5
-
Nuur Athirah Binti Mohd Daud
+/., -/.
3
11
c.1617C>T
p.Pro539Pro
r.(=)
p.(=)
-
Benign,
ClinVar
g.11116124C>T
N510N
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
,
1 more item
LDLR_000014
rs5929
4/33, 6/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/., ./.
2
11i
c.1705+56C>T
-
r.(=)
p.(=)
-
Likely benign,
ClinVar
g.11116268C>T
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000015
rs4508523
12/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/., -?/.
2
11i
c.1705+112C>G
-
r.(=)
p.(=)
-
Likely benign,
ClinVar
g.11116324C>G
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000016
rs879254995
1/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/.
2
11i
c.1705+117T>G
-
r.(=)
p.(=)
-
-
g.11116329T>G
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
LDLR_000019
-
2/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
-/.
1
11i
c.1706-69G>T
-
r.(=)
p.(=)
-
ClinVar
g.11116790G>T
-
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000018
rs7259278
1/147
-
Nuur Athirah Binti Mohd Daud
-/.
1
11i
c.1706-55A>C
-
r.(=)
p.(=)
-
ClinVar
g.11116804A>C
-
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000017
rs2738447
6/147
-
Nuur Athirah Binti Mohd Daud
+/.
1
12
c.1706_1845dup
-
r.(?)
p.(Asp616Ilefs*96)
-
-
g.11116859_11116998dup
-
Alyaa Al-Khateeb et al. (2011)
LDLR_000028
-
2/147
-
Nuur Athirah Binti Mohd Daud
./.
1
12
c.1729T>C
-
r.(?)
p.(Trp577Arg)
-
ClinVar
g.11116882T>C
p.Trp576Arg in exon 12
Kah Lin Khoo et al. (2016)
,
dbSNP
,
ClinVar
LDLR_000056
rs879255000
1/5
-
Nuur Athirah Binti Mohd Daud
+/., ./.
4
12, 12i
c.1773C>T
p.Asn591Asn
r.(=)
p.(=)
-
Benign/Likely benign,
ClinVar
g.11116926C>T
c.1773T>C, N570N
dbSNP
,
ClinVar
, {DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
2 more items
LDLR_000020
rs688
19/40, 5/33, 7/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
./.
2
13
c.1959T>C
-
r.(=)
p.(=)
-
ClinVar
g.11120205T>C
V632V
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
,
M Azian et al. (2006)
,
dbSNP
,
ClinVar
LDLR_000021
rs5925
1/147, 7/33
-
Nuur Athirah Binti Mohd Daud
+/.
1
14
c.1996_2012del
-
r.(?)
p.(Trp666Profs*45)
-
ClinVar
g.11120378_11120394del
c.1996_2012del17
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000030
rs879255104
4/147
-
Nuur Athirah Binti Mohd Daud
+/.
1
14
c.2050G>A
-
r.(?)
p.(Ala684Thr)
-
ClinVar
g.11120432G>A
GCC>ACC at 2048
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
LDLR_000044
rs774730452
1/9
-
Nuur Athirah Binti Mohd Daud
+/.
1
14
c.2087G>A
-
r.(?)
p.(Cys696Tyr)
-
ClinVar
g.11120469G>A
TGC>TAC at 2087
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
LDLR_000043
rs879255134
1/9
-
Nuur Athirah Binti Mohd Daud
./.
1
14
c.2100C>G
-
r.(?)
p.(Asp700Glu)
-
ClinVar
g.11120482C>G
-
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000029
rs759858813
5/147
-
Nuur Athirah Binti Mohd Daud
+/.
1
14
c.2108_2114dup
-
r.(?)
p.(Arg706Alafs*13)
-
ClinVar
g.11120490_11120496dup
TGCTGGCins2108
K L Khoo et al. (2000)
,
dbSNP
,
ClinVar
LDLR_000050
rs879255141
1/10
-
Nuur Athirah Binti Mohd Daud
+/., +?/.
4
14
c.2132G>A
-
r.(?)
p.(Cys711Tyr)
-
Likely pathogenic,
ClinVar
g.11120514G>A
Cys711Tyr in exon 14
J K Chahil et al.(2012)
,
Kah Lin Khoo et al. (2016)
,
dbSNP
,
ClinVar
LDLR_000052
rs879255145
1, 3/10
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
-?/.
1
15
c.2209A>G
-
r.(?)
p.(Arg737Gly)
-
ClinVar
g.11123242A>G
R716G
M Azian et al. (2006)
,
dbSNP
,
ClinVar
LDLR_000058
rs879255165
1/33
-
Nuur Athirah Binti Mohd Daud
+/., -/.
2
15
c.2232A>G
p.Arg744Arg
r.(=)
p.(=)
-
Benign,
ClinVar
g.11123265A>G
-
{DOI:Nor Idahriani Muhd Nor:10.35119/MYJO.V1I2.18},
Alyaa Al-Khateeb et al. (2011)
,
dbSNP
,
ClinVar
LDLR_000022
rs5927
5/147
-
Nuur Athirah Binti Mohd Daud
,
Nur Aisyah Athirah
+/.
1
15i
c.2311+1G>T
-
r.spl?
p.?
-
-
g.11123345G>T
c.2311+1 G to T in intron 15
Kah Lin Khoo et al. (2016)
,
ClinVar
LDLR_000057
-
1/2
-
Nuur Athirah Binti Mohd Daud
+?/.
1
15i
c.2312-1679T>C
-
r.(=)
p.(=)
-
-
g.11126329T>C
-
Livy Alex et al. (2012)
,
dbSNP
LDLR_000034
rs10422244
1/2
-
Nuur Athirah Binti Mohd Daud
+/.
1
16
c.2389G>A
-
r.(?)
p.(Val797Met)
-
-
g.11128085G>A
Val797Met in exon 16
Kah Lin Khoo et al. (2016)
,
ClinVar
LDLR_000054
-
1/10
-
Nuur Athirah Binti Mohd Daud
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