Individual #00000265

Reference	Sathiya Maran et al. (2020)
Gender	-
Geographic origin	Malaysia
Ethnic origin	-
Population	-
Remarks	-
Microattribution	-
Panel size	1
Diseases	ASD
Owner name	Nuur Athirah Binti Mohd Daud
Database submission license
Created by	Nuur Athirah Binti Mohd Daud
Date created	2020-12-16 16:00:05 +08:00 (CST)
Date last edited	2020-12-20 10:25:50 +08:00 (CST)

No phenotypes found for this individual!

Screenings

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DNA
RNA = RNA (cDNA)
Protein
? = unknown

Technique: Technique(s) used to identify the sequence variant.
All options:

? = Unknown
arrayCGH = array for Comparative Genomic Hybridisation
arraySEQ = array for resequencing
arraySNP = array for SNP typing
arrayCNV = array for Copy Number Variation (SNP and CNV probes)
BESS = Base Excision Sequence Scanning
CMC = Chemical Mismatch Cleavage
CSCE = Conformation Sensitive Capillary Electrophoresis
DGGE = Denaturing-Gradient Gel-Electrophoresis
DHPLC = Denaturing High-Performance Liquid Chromatography
DOVAM = Detection Of Virtually All Mutations (SSCA variant)
ddF = dideoxy Fingerprinting
DSCA = Double-Strand DNA Conformation Analysis
EMC = Enzymatic Mismatch Cleavage
HD = HeteroDuplex analysis
MCA = high-resolution Melting Curve Analysis (hrMCA)
IHC = Immuno-Histo-Chemistry
MAPH = Multiplex Amplifiable Probe Hybridisation
MLPA = Multiplex Ligation-dependent Probe Amplification
SEQ-NG = Next-Generation Sequencing
SEQ-NG-H = Next-Generation Sequencing - Helicos
SEQ-NG-I = Next-Generation Sequencing - Illumina/Solexa
SEQ-NG-R = Next-Generation Sequencing - Roche/454
SEQ-NG-S = Next-Generation Sequencing - SOLiD
Northern = Northern blotting
PCR = Polymerase Chain Reaction
PCRdig = PCR + restriction enzyme digestion
PCRlr = PCR, long-range
PCRm = PCR, multiplex
PCRq = PCR, quantitative
PAGE = Poly-Acrylamide Gel-Electrophoresis
PTT = Protein Truncation Test
PFGE = Pulsed-Field Gel-Electrophoresis (+Southern)
RT-PCR = Reverse Transcription and PCR
SEQ = SEQuencing
SBE = Single Base Extension
SSCA = Single-Strand DNA Conformation polymorphism Analysis (SSCP)
SSCAf = SSCA, fluorescent (SSCP)
Southern = Southern blotting
TaqMan = TaqMan assay
Western = Western Blotting

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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'
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^	Text	^p.(Arg	all entries beginning with 'p.(Arg'
$	Text	Ser)$	all entries ending with 'Ser)'
=""	Text	=""	all entries with this field empty
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combination	Text	*\|Ter !fs	all entries containing '*' or 'Ter' but not containing 'fs'
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\|	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
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>=	Numeric	>=23	all entries higher than, or equal to, 23
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Example	Matches
Asian	all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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"South Asian"	all entries containing 'South Asian', but not containing 'South East Asian'

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Screening ID	Template	Technique	Genes screened	Variants found	Owner
0000000280	DNA	SEQ-NG-I;PCRlr	MYH3	21	Nuur Athirah Binti Mohd Daud

Variants

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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.

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.

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.

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.

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

21 entries on 1 page. Showing entries 1 - 21.

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How to query

Chr	Allele	Effect	DNA change (genomic) (hg38)	Published as	Reference	DB-ID	dbSNP ID	Frequency	Variant remarks	Owner	Gene	Exon	DNA change (cDNA)	Published as	RNA change	Protein	GVS function	Clinical classification
17	Unknown	./.	g.10630279dup	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000011	rs397750512	33/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.5457+9dup	-	r.(=)	p.(=)	-	ClinVar
17	Unknown	-/.	g.10631643C>T	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000004	rs34393601	2/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.5254G>A	-	r.(?)	p.(Ala1752Thr)	-	ClinVar
17	Both (homozygous)	-/.	g.10632032C>A	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000005	rs2239936	14/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.4957-16G>T	-	r.(=)	p.(=)	-	ClinVar
17	Unknown	-/.	g.10632032C>A	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000005	rs2239936	21/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.4957-16G>T	-	r.(=)	p.(=)	-	ClinVar
17	Unknown	+/.	g.10632701G>A	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000009	rs2285479	24/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.4731C>T	-	r.(=)	p.(=)	-	ClinVar
17	Both (homozygous)	-/.	g.10632701G>A	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000009	rs2285479	10/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.4731C>T	-	r.(=)	p.(=)	-	ClinVar
17	Both (homozygous)	+/.	g.10632918T>C	-	Sathiya Maran et al. (2020), dbSNP	MYH3_000003	rs1981514	8/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.4648-134A>G	-	r.(=)	p.(=)	-	-
17	Unknown	+/.	g.10632918T>C	-	Sathiya Maran et al. (2020), dbSNP	MYH3_000003	rs1981514	20/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.4648-134A>G	-	r.(=)	p.(=)	-	-
17	Unknown	+/.	g.10636778T>G	-	Sathiya Maran et al. (2020), dbSNP	MYH3_000010	rs55980976	21/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.3857-925A>C	-	r.(=)	p.(=)	-	-
17	Both (homozygous)	+/.	g.10636778T>G	-	Sathiya Maran et al. (2020), dbSNP	MYH3_000010	rs55980976	9/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.3857-925A>C	-	r.(=)	p.(=)	-	-
17	Both (homozygous)	-/.	g.10638198C>T	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000008	rs2285477	4/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.3574G>A	-	r.(?)	p.(Ala1192Thr)	-	ClinVar
17	Unknown	-/.	g.10638198C>T	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000008	rs2285477	20/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.3574G>A	-	r.(?)	p.(Ala1192Thr)	-	ClinVar
17	Both (homozygous)	-/.	g.10639448A>G	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000002	rs2285474	7/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.2952T>C	-	r.(=)	p.(=)	-	ClinVar
17	Unknown	-/.	g.10639448A>G	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000002	rs2285474	17/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.2952T>C	-	r.(=)	p.(=)	-	ClinVar
17	Both (homozygous)	-/.	g.10639486T>C	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000007	rs2285473	3/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.2926-12A>G	-	r.(=)	p.(=)	-	ClinVar
17	Unknown	-/.	g.10639486T>C	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000007	rs2285473	19/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.2926-12A>G	-	r.(=)	p.(=)	-	ClinVar
17	Unknown	-/.	g.10639569T>C	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000006	rs2285472	19/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.2916A>G	-	r.(=)	p.(=)	-	ClinVar
17	Both (homozygous)	-/.	g.10639569T>C	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000006	rs2285472	4/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.2916A>G	-	r.(=)	p.(=)	-	ClinVar
17	Both (homozygous)	-?/.	g.10651704T>C	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000012	rs2285467	1/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.349-36A>G	-	r.(=)	p.(=)	-	ClinVar
17	Unknown	-?/.	g.10651704T>C	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000012	rs2285467	12/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.349-36A>G	-	r.(=)	p.(=)	-	ClinVar
17	Unknown	./.	g.10655059A>G	-	Sathiya Maran et al. (2020), dbSNP, ClinVar	MYH3_000001	rs17817203	2/51	-	Nuur Athirah Binti Mohd Daud	MYH3	-	NM_002470.3:c.6T>C	-	r.(=)	p.(=)	-	ClinVar

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