NM_016341.4(PLCE1):c.6720+49dup AND not provided

Germline classification:: Benign (1 submission)
Last evaluated:: Aug 26, 2021
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

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:: RCV001665253.2

Allele description [Variation Report for NM_016341.4(PLCE1):c.6720+49dup]

NM_016341.4(PLCE1):c.6720+49dup

Genes:

NOC3L:NOC3 like DNA replication regulator [Gene - OMIM - HGNC]
PLCE1:phospholipase C epsilon 1 [Gene - OMIM - HGNC]

Variant type:

Duplication

Cytogenetic location:

10q23.33

Genomic location:

Preferred name:

NM_016341.4(PLCE1):c.6720+49dup

HGVS:

NC_000010.11:g.94324616dup
NG_015799.1:g.335628dup
NM_001165979.2:c.5796+49dup
NM_001288989.2:c.6672+49dup
NM_016341.4:c.6720+49dupMANE SELECT
NC_000010.10:g.96084373dup
NM_016341.4:c.6720+49dupTMANE SELECT

Links:

dbSNP: rs3831084

NCBI 1000 Genomes Browser:

rs3831084

Molecular consequence:

NM_001165979.2:c.5796+49dup - intron variant - [Sequence Ontology: SO:0001627]
NM_001288989.2:c.6672+49dup - intron variant - [Sequence Ontology: SO:0001627]
NM_016341.4:c.6720+49dup - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: C3661900

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001875001	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Aug 26, 2021)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001875001

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Aug 26, 2021)

germline

clinical testing

Citation Link

Help

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001875001.1

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

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

Last Updated: Jul 29, 2024

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