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NM_002397.5(MEF2C):c.1319G>A (p.Arg440Gln) AND Intellectual disability, autosomal dominant 20

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Apr 5, 2020
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:
RCV001332879.1

Allele description [Variation Report for NM_002397.5(MEF2C):c.1319G>A (p.Arg440Gln)]

NM_002397.5(MEF2C):c.1319G>A (p.Arg440Gln)

Genes:
MEF2C-AS2:MEF2C antisense RNA 2 [Gene - HGNC]
MEF2C:myocyte enhancer factor 2C [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
5q14.3
Genomic location:
Preferred name:
NM_002397.5(MEF2C):c.1319G>A (p.Arg440Gln)
HGVS:
  • NC_000005.10:g.88722707C>T
  • NG_023427.1:g.186399G>A
  • NM_001131005.2:c.1289G>A
  • NM_001193347.1:c.1349G>A
  • NM_001193348.1:c.1151G>A
  • NM_001193349.3:c.1079G>A
  • NM_001193350.2:c.1319G>A
  • NM_001308002.3:c.1295G>A
  • NM_001363581.2:c.1223G>A
  • NM_001364329.2:c.1319G>A
  • NM_001364330.2:c.1319G>A
  • NM_001364331.2:c.1319G>A
  • NM_001364332.2:c.1079G>A
  • NM_001364333.2:c.1295G>A
  • NM_001364334.2:c.1223G>A
  • NM_001364335.2:c.1223G>A
  • NM_001364336.2:c.1223G>A
  • NM_001364337.2:c.1223G>A
  • NM_001364338.2:c.1253G>A
  • NM_001364339.2:c.1199G>A
  • NM_001364340.2:c.1199G>A
  • NM_001364341.2:c.1199G>A
  • NM_001364342.2:c.1199G>A
  • NM_001364343.2:c.1193G>A
  • NM_001364344.2:c.1175G>A
  • NM_001364345.2:c.*54G>A
  • NM_001364346.2:c.*54G>A
  • NM_001364347.2:c.*54G>A
  • NM_001364348.2:c.*54G>A
  • NM_001364349.2:c.*54G>A
  • NM_001364350.2:c.*54G>A
  • NM_001364352.2:c.*54G>A
  • NM_001364353.2:c.941G>A
  • NM_001364354.2:c.*54G>A
  • NM_001364355.2:c.*54G>A
  • NM_001364356.2:c.845G>A
  • NM_001364357.2:c.773G>A
  • NM_002397.5:c.1319G>AMANE SELECT
  • NP_001124477.1:p.Arg430Gln
  • NP_001180276.1:p.Arg450Gln
  • NP_001180277.1:p.Arg384Gln
  • NP_001180278.1:p.Arg360Gln
  • NP_001180279.1:p.Arg440Gln
  • NP_001294931.1:p.Arg432Gln
  • NP_001350510.1:p.Arg408Gln
  • NP_001351258.1:p.Arg440Gln
  • NP_001351259.1:p.Arg440Gln
  • NP_001351260.1:p.Arg440Gln
  • NP_001351261.1:p.Arg360Gln
  • NP_001351262.1:p.Arg432Gln
  • NP_001351263.1:p.Arg408Gln
  • NP_001351264.1:p.Arg408Gln
  • NP_001351265.1:p.Arg408Gln
  • NP_001351266.1:p.Arg408Gln
  • NP_001351267.1:p.Arg418Gln
  • NP_001351268.1:p.Arg400Gln
  • NP_001351269.1:p.Arg400Gln
  • NP_001351270.1:p.Arg400Gln
  • NP_001351271.1:p.Arg400Gln
  • NP_001351272.1:p.Arg398Gln
  • NP_001351273.1:p.Arg392Gln
  • NP_001351282.1:p.Arg314Gln
  • NP_001351285.1:p.Arg282Gln
  • NP_001351286.1:p.Arg258Gln
  • NP_002388.2:p.Arg440Gln
  • NC_000005.9:g.88018524C>T
  • NR_146284.1:n.339C>T
Protein change:
R258Q
Links:
dbSNP: rs1360994640
NCBI 1000 Genomes Browser:
rs1360994640
Molecular consequence:
  • NM_001364345.2:c.*54G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001364346.2:c.*54G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001364347.2:c.*54G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001364348.2:c.*54G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001364349.2:c.*54G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001364350.2:c.*54G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001364352.2:c.*54G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001364354.2:c.*54G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001364355.2:c.*54G>A - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001131005.2:c.1289G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001193347.1:c.1349G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001193348.1:c.1151G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001193349.3:c.1079G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001193350.2:c.1319G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001308002.3:c.1295G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001363581.2:c.1223G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364329.2:c.1319G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364330.2:c.1319G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364331.2:c.1319G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364332.2:c.1079G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364333.2:c.1295G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364334.2:c.1223G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364335.2:c.1223G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364336.2:c.1223G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364337.2:c.1223G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364338.2:c.1253G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364339.2:c.1199G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364340.2:c.1199G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364341.2:c.1199G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364342.2:c.1199G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364343.2:c.1193G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364344.2:c.1175G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364353.2:c.941G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364356.2:c.845G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001364357.2:c.773G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_002397.5:c.1319G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_146284.1:n.339C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Intellectual disability, autosomal dominant 20 (NEDHSIL)
Synonyms:
NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE
Identifiers:
MONDO: MONDO:0013266; MedGen: C3150700; Orphanet: 228384; OMIM: 613443

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001525318Baylor Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Apr 5, 2020) 		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 Baylor Genetics, SCV001525318.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 16, 2024