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NM_001110792.2(MECP2):c.710C>G (p.Pro237Arg) AND multiple conditions

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Jan 1, 2017
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:
RCV000626873.3

Allele description [Variation Report for NM_001110792.2(MECP2):c.710C>G (p.Pro237Arg)]

NM_001110792.2(MECP2):c.710C>G (p.Pro237Arg)

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.710C>G (p.Pro237Arg)
Other names:
NM_001110792.2(MECP2):c.710C>G; p.Pro237Arg
HGVS:
  • NC_000023.11:g.154031154G>C
  • NG_007107.3:g.110950C>G
  • NM_001110792.2:c.710C>GMANE SELECT
  • NM_001316337.2:c.395C>G
  • NM_001369391.2:c.395C>G
  • NM_001369392.2:c.395C>G
  • NM_001369393.2:c.395C>G
  • NM_001369394.2:c.395C>G
  • NM_001386137.1:c.5C>G
  • NM_001386138.1:c.5C>G
  • NM_001386139.1:c.5C>G
  • NM_004992.4:c.674C>G
  • NP_001104262.1:p.Pro237Arg
  • NP_001303266.1:p.Pro132Arg
  • NP_001356320.1:p.Pro132Arg
  • NP_001356321.1:p.Pro132Arg
  • NP_001356322.1:p.Pro132Arg
  • NP_001356323.1:p.Pro132Arg
  • NP_001373066.1:p.Pro2Arg
  • NP_001373067.1:p.Pro2Arg
  • NP_001373068.1:p.Pro2Arg
  • NP_004983.1:p.Pro225Arg
  • NP_004983.1:p.Pro225Arg
  • LRG_764t1:c.710C>G
  • LRG_764t2:c.674C>G
  • AJ132917.1:c.674C>G
  • LRG_764:g.110950C>G
  • LRG_764p1:p.Pro237Arg
  • LRG_764p2:p.Pro225Arg
  • NC_000023.10:g.153296605G>C
  • NG_007107.2:g.110974C>G
  • NM_004992.3:c.674C>G
  • P51608:p.Pro225Arg
Protein change:
P132R
Links:
UniProtKB: P51608#VAR_018198; dbSNP: rs61749715
NCBI 1000 Genomes Browser:
rs61749715
Molecular consequence:
  • NM_001110792.2:c.710C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001316337.2:c.395C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001369391.2:c.395C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001369392.2:c.395C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001369393.2:c.395C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001369394.2:c.395C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001386137.1:c.5C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001386138.1:c.5C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001386139.1:c.5C>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004992.4:c.674C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Seizure
Synonyms:
Seizures
Identifiers:
MedGen: C0036572; Human Phenotype Ontology: HP:0001250
Name:
Absent speech
Synonyms:
Absent speech development
Identifiers:
MedGen: C1854882; Human Phenotype Ontology: HP:0001344
Name:
Developmental regression
Synonyms:
C1836830
Identifiers:
MedGen: C1836830; Human Phenotype Ontology: HP:0002376
Name:
Severe global developmental delay
Synonyms:
Severe psychomotor retardation
Identifiers:
MedGen: C1837397; Human Phenotype Ontology: HP:0011344
Name:
Irregular respiration
Identifiers:
MedGen: C0425492; Human Phenotype Ontology: HP:0012195

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000747576Centre for Mendelian Genomics, University Medical Centre Ljubljana
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(Jan 1, 2017) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownyesnot providednot providednot providednot providednot providedclinical testing

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 Centre for Mendelian Genomics, University Medical Centre Ljubljana, SCV000747576.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 10, 2024