NM_000435.3(NOTCH3):c.1162T>C (p.Cys388Arg) AND multiple conditions

Germline classification:: Likely pathogenic (1 submission)
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV001003545.1

Allele description [Variation Report for NM_000435.3(NOTCH3):c.1162T>C (p.Cys388Arg)]

NM_000435.3(NOTCH3):c.1162T>C (p.Cys388Arg)

Gene:

NOTCH3:notch receptor 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.12

Genomic location:

Preferred name:

NM_000435.3(NOTCH3):c.1162T>C (p.Cys388Arg)

HGVS:

NC_000019.10:g.15189303A>G
NG_009819.1:g.16679T>C
NM_000435.3:c.1162T>CMANE SELECT
NP_000426.2:p.Cys388Arg
NC_000019.9:g.15300114A>G
NM_000435.2:c.1162T>C

Protein change:

C388R

Links:

dbSNP: rs1599391938

NCBI 1000 Genomes Browser:

rs1599391938

Molecular consequence:

NM_000435.3:c.1162T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Migraine with aura
Identifiers:: MONDO: MONDO:0005475; MedGen: C0154723; Human Phenotype Ontology: HP:0002077

Name:: Abnormal cerebral white matter morphology
Synonyms:: Abnormality of the cerebral white matter
Identifiers:: MedGen: C0948163; Human Phenotype Ontology: HP:0002500

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001161889	NIHR Bioresource Rare Diseases, University of Cambridge	no assertion criteria provided	Likely pathogenic	unknown	research	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001161889

NIHR Bioresource Rare Diseases, University of Cambridge

no assertion criteria provided

Likely pathogenic

unknown

research

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	unknown	yes	1	not provided	not provided	1	not provided	research

Citations

PubMed

Whole-genome sequencing of patients with rare diseases in a national health system.

Turro E, Astle WJ, Megy K, Gräf S, Greene D, Shamardina O, Allen HL, Sanchis-Juan A, Frontini M, Thys C, Stephens J, Mapeta R, Burren OS, Downes K, Haimel M, Tuna S, Deevi SVV, Aitman TJ, Bennett DL, Calleja P, Carss K, Caulfield MJ, et al.

Nature. 2020 Jul;583(7814):96-102. doi: 10.1038/s41586-020-2434-2. Epub 2020 Jun 24.

PubMed [citation]

PMID:: 32581362
PMCID:: PMC7610553

Details of each submission

From NIHR Bioresource Rare Diseases, University of Cambridge, SCV001161889.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	1	not provided	not provided	research	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	unknown	yes	1	not provided	not provided		1	not provided	not provided	not provided

Last Updated: Apr 23, 2022

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