NM_181332.3(NLGN4X):c.2444G>C (p.Arg815Thr) AND not provided

This record was updated by the submitter. Please see the current version.

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 18, 2019
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:: RCV001756425.1

Allele description

NM_181332.3(NLGN4X):c.2444G>C (p.Arg815Thr)

Gene:

NLGN4X:neuroligin 4 X-linked [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xp22.32

Genomic location:

Preferred name:

NM_181332.3(NLGN4X):c.2444G>C (p.Arg815Thr)

HGVS:

NC_000023.11:g.5892824C>G
NG_008881.2:g.341059G>C
NM_001282145.2:c.2444G>C
NM_001282146.2:c.2444G>C
NM_020742.4:c.2444G>C
NM_181332.3:c.2444G>CMANE SELECT
NP_001269074.1:p.Arg815Thr
NP_001269075.1:p.Arg815Thr
NP_065793.1:p.Arg815Thr
NP_851849.1:p.Arg815Thr
NC_000023.10:g.5810865C>G
NM_020742.2:c.2444G>C

Protein change:

R815T

Molecular consequence:

NM_001282145.2:c.2444G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_001282146.2:c.2444G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_020742.4:c.2444G>C - missense variant - [Sequence Ontology: SO:0001583]
NM_181332.3:c.2444G>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:: none provided
Identifiers:: MedGen: CN517202

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001985177	GeneDx	criteria provided, single submitter (GeneDX Variant Classification (06012015))	Uncertain significance (Oct 18, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001985177

GeneDx

criteria provided, single submitter

(GeneDX Variant Classification (06012015))

Uncertain significance
(Oct 18, 2019)

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, SCV001985177.1

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

Description

In silico analysis, which includes protein predictors and evolutionary conservation, supports a deleterious effect; Has not been previously published as pathogenic or benign to our knowledge

#	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: Apr 23, 2022

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Relating variation to medicine