NM_001110792.2(MECP2):c.719C>G (p.Thr240Ser) AND not provided

Germline classification:: Benign (2 submissions)
Last evaluated:: Mar 3, 2015
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV001705937.3

Allele description [Variation Report for NM_001110792.2(MECP2):c.719C>G (p.Thr240Ser)]

NM_001110792.2(MECP2):c.719C>G (p.Thr240Ser)

Gene:

MECP2:methyl-CpG binding protein 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

Xq28

Genomic location:

Preferred name:

NM_001110792.2(MECP2):c.719C>G (p.Thr240Ser)

Other names:

NM_001110792.2(MECP2):c.719C>G; p.Thr240Ser

HGVS:

NC_000023.11:g.154031145G>C
NG_007107.3:g.110959C>G
NM_001110792.2:c.719C>GMANE SELECT
NM_001316337.2:c.404C>G
NM_001369391.2:c.404C>G
NM_001369392.2:c.404C>G
NM_001369393.2:c.404C>G
NM_001369394.2:c.404C>G
NM_001386137.1:c.14C>G
NM_001386138.1:c.14C>G
NM_001386139.1:c.14C>G
NM_004992.4:c.683C>G
NP_001104262.1:p.Thr240Ser
NP_001303266.1:p.Thr135Ser
NP_001356320.1:p.Thr135Ser
NP_001356321.1:p.Thr135Ser
NP_001356322.1:p.Thr135Ser
NP_001356323.1:p.Thr135Ser
NP_001373066.1:p.Thr5Ser
NP_001373067.1:p.Thr5Ser
NP_001373068.1:p.Thr5Ser
NP_004983.1:p.Thr228Ser
NP_004983.1:p.Thr228Ser
LRG_764t1:c.719C>G
LRG_764t2:c.683C>G
AJ132917.1:c.683C>G
LRG_764:g.110959C>G
LRG_764p1:p.Thr240Ser
LRG_764p2:p.Thr228Ser
NC_000023.10:g.153296596G>C
NG_007107.2:g.110983C>G
NM_001110792.1:c.719C>G
NM_004992.3:c.683C>G
P51608:p.Thr228Ser

Protein change:

T135S

Links:

UniProtKB: P51608#VAR_018199; dbSNP: rs61749738

NCBI 1000 Genomes Browser:

rs61749738

Molecular consequence:

NM_001110792.2:c.719C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001316337.2:c.404C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369391.2:c.404C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369392.2:c.404C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369393.2:c.404C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001369394.2:c.404C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386137.1:c.14C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386138.1:c.14C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001386139.1:c.14C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_004992.4:c.683C>G - missense variant - [Sequence Ontology: SO:0001583]

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
SCV001838739	GeneDx	criteria provided, single submitter (GeneDx Variant Classification Process June 2021)	Benign (Mar 3, 2015)	germline	clinical testing	Citation Link,
SCV005275063	Breakthrough Genomics, Breakthrough Genomics	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign	germline	not provided	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001838739

GeneDx

criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)

Benign
(Mar 3, 2015)

germline

clinical testing

Citation Link,

SCV005275063

Breakthrough Genomics, Breakthrough Genomics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign

germline

not provided

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	germline	yes	not provided	not provided	not provided	not provided	not provided	clinical testing, not provided

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From GeneDx, SCV001838739.1

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

Description

This variant is associated with the following publications: (PMID: 23810759, 12111644)

#	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

From Breakthrough Genomics, Breakthrough Genomics, SCV005275063.1

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

#	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: Nov 10, 2024

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