NM_015175.3(NBEAL2):c.-178G>A AND Gray platelet syndrome

Clinical significance:Uncertain significance (Last evaluated: Jan 13, 2018)
Review status:1 star out of maximum of 4 stars
criteria provided, single submitter

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Based on:: 1 submission [Details]
Record status:: current
Accession:: RCV001144235.5

Allele description [Variation Report for NM_015175.3(NBEAL2):c.-178G>A]

NM_015175.3(NBEAL2):c.-178G>A

Genes:

CCDC12:coiled-coil domain containing 12 [Gene - HGNC]
NBEAL2:neurobeachin like 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p21.31

Genomic location:

Preferred name:

NM_015175.3(NBEAL2):c.-178G>A

HGVS:

NC_000003.12:g.46979684G>A
NG_031914.1:g.5002G>A
NM_015175.3:c.-178G>AMANE SELECT
NM_144716.6:c.-73+2248C>T
LRG_568t1:c.-178G>A
LRG_568:g.5002G>A
NC_000003.11:g.47021174G>A
NM_015175.2:c.-178G>A

Links:

dbSNP: rs892777590

NCBI 1000 Genomes Browser:

rs892777590

Molecular consequence:

NM_015175.3:c.-178G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_144716.6:c.-73+2248C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Gray platelet syndrome (GPS)
Synonyms:: Platelet alpha-granule deficiency; Marked decrease or absence of alpha-granules and of platelet-specific alpha-granule proteins; BLEEDING DISORDER, PLATELET-TYPE, 4
Identifiers:: MONDO: MONDO:0007686; MedGen: C0272302; Orphanet: 721; OMIM: 139090

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001304823	Illumina Laboratory Services, Illumina	criteria provided, single submitter ICSL Variant Classification Criteria 13 December 2019	Uncertain significance (Jan 13, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001304823

Illumina Laboratory Services, Illumina

criteria provided, single submitter

ICSL Variant Classification Criteria 13 December 2019

Uncertain significance
(Jan 13, 2018)

germline

clinical testing

Citation Link

Summary from all submissions

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Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Illumina Laboratory Services, Illumina, SCV001304823.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

This variant was observed in the ICSL laboratory as part of a predisposition screen in an ostensibly healthy population. It had not been previously curated by ICSL or reported in the Human Gene Mutation Database (HGMD: prior to June 1st, 2018), and was therefore a candidate for classification through an automated scoring system. Utilizing variant allele frequency, disease prevalence and penetrance estimates, and inheritance mode, an automated score was calculated to assess if this variant is too frequent to cause the disease. Based on the score, this variant could not be ruled out of causing disease and therefore its association with disease required further investigation. A literature search was performed for the gene, cDNA change, and amino acid change (if applicable). No publications were found based on this search. This variant was therefore classified as a variant of unknown significance for this disease.

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

Last Updated: Mar 18, 2023

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