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NM_001326342.2(CELF2):c.241_262dup (p.Gln88fs) AND Developmental and epileptic encephalopathy 97

Germline classification:
Likely pathogenic (1 submission)
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:
RCV004782232.1

Allele description [Variation Report for NM_001326342.2(CELF2):c.241_262dup (p.Gln88fs)]

NM_001326342.2(CELF2):c.241_262dup (p.Gln88fs)

Gene:
CELF2:CUGBP Elav-like family member 2 [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
10p14
Genomic location:
Preferred name:
NM_001326342.2(CELF2):c.241_262dup (p.Gln88fs)
HGVS:
  • NC_000010.11:g.11165652_11165673dup
  • NG_182741.1:g.41_62dup
  • NM_001025076.2:c.148_169dup
  • NM_001025077.3:c.220_241dup
  • NM_001083591.1:c.148_169dup
  • NM_001326317.2:c.148_169dup
  • NM_001326318.2:c.148_169dup
  • NM_001326319.2:c.148_169dup
  • NM_001326320.2:c.148_169dup
  • NM_001326321.2:c.148_169dup
  • NM_001326323.2:c.148_169dup
  • NM_001326324.2:c.148_169dup
  • NM_001326325.2:c.313_334dup
  • NM_001326326.2:c.256_277dup
  • NM_001326327.2:c.256_277dup
  • NM_001326328.2:c.148_169dup
  • NM_001326329.2:c.148_169dup
  • NM_001326330.2:c.148_169dup
  • NM_001326331.2:c.220_241dup
  • NM_001326332.2:c.220_241dup
  • NM_001326333.2:c.-385_-364dup
  • NM_001326334.2:c.148_169dup
  • NM_001326335.2:c.220_241dup
  • NM_001326336.2:c.220_241dup
  • NM_001326337.2:c.220_241dup
  • NM_001326338.2:c.-31_-10dup
  • NM_001326339.2:c.-31_-10dup
  • NM_001326340.2:c.241_262dup
  • NM_001326341.2:c.241_262dup
  • NM_001326342.2:c.241_262dupMANE SELECT
  • NM_001326343.2:c.241_262dup
  • NM_001326344.2:c.148_169dup
  • NM_001326345.2:c.148_169dup
  • NM_001326346.2:c.-302_-281dup
  • NM_001326347.1:c.172_193dup
  • NM_001326348.2:c.148_169dup
  • NM_001326349.2:c.148_169dup
  • NM_001394502.1:c.220_241dup
  • NM_001394513.1:c.241_262dup
  • NM_001394517.1:c.148_169dup
  • NM_001394518.1:c.241_262dup
  • NM_001394519.1:c.241_262dup
  • NM_006561.4:c.241_262dup
  • NP_001020247.1:p.Gln57fs
  • NP_001020248.1:p.Gln81fs
  • NP_001077060.1:p.Gln57fs
  • NP_001313246.1:p.Gln57fs
  • NP_001313247.1:p.Gln57fs
  • NP_001313248.1:p.Gln57fs
  • NP_001313249.1:p.Gln57fs
  • NP_001313250.1:p.Gln57fs
  • NP_001313252.1:p.Gln57fs
  • NP_001313253.1:p.Gln57fs
  • NP_001313254.1:p.Gln112fs
  • NP_001313255.1:p.Gln93fs
  • NP_001313256.1:p.Gln93fs
  • NP_001313257.1:p.Gln57fs
  • NP_001313258.1:p.Gln57fs
  • NP_001313259.1:p.Gln57fs
  • NP_001313260.1:p.Gln81fs
  • NP_001313261.1:p.Gln81fs
  • NP_001313263.1:p.Gln57fs
  • NP_001313264.1:p.Gln81fs
  • NP_001313265.1:p.Gln81fs
  • NP_001313266.1:p.Gln81fs
  • NP_001313269.1:p.Gln88fs
  • NP_001313270.1:p.Gln88fs
  • NP_001313271.1:p.Gln88fs
  • NP_001313272.1:p.Gln88fs
  • NP_001313273.1:p.Gln57fs
  • NP_001313274.1:p.Gln57fs
  • NP_001313276.1:p.Gln65fs
  • NP_001313277.1:p.Gln57fs
  • NP_001313278.1:p.Gln57fs
  • NP_001381431.1:p.Gln81fs
  • NP_001381442.1:p.Gln88fs
  • NP_001381446.1:p.Gln57fs
  • NP_001381447.1:p.Gln88fs
  • NP_001381448.1:p.Gln88fs
  • NP_006552.3:p.Gln88fs
  • NC_000010.10:g.11207615_11207636dup
Protein change:
Q112fs
Molecular consequence:
  • NM_001326333.2:c.-385_-364dup - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001326338.2:c.-31_-10dup - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001326339.2:c.-31_-10dup - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001326346.2:c.-302_-281dup - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001025076.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001025077.3:c.220_241dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001083591.1:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326317.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326318.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326319.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326320.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326321.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326323.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326324.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326325.2:c.313_334dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326326.2:c.256_277dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326327.2:c.256_277dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326328.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326329.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326330.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326331.2:c.220_241dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326332.2:c.220_241dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326334.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326335.2:c.220_241dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326336.2:c.220_241dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326337.2:c.220_241dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326340.2:c.241_262dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326341.2:c.241_262dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326342.2:c.241_262dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326343.2:c.241_262dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326344.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326345.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326347.1:c.172_193dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326348.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001326349.2:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001394502.1:c.220_241dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001394513.1:c.241_262dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001394517.1:c.148_169dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001394518.1:c.241_262dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001394519.1:c.241_262dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_006561.4:c.241_262dup - frameshift variant - [Sequence Ontology: SO:0001589]

Condition(s)

Name:
Developmental and epileptic encephalopathy 97 (DEE97)
Identifiers:
MONDO: MONDO:0030453; MedGen: C5561999; OMIM: 619561

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005395952Equipe Genetique des Anomalies du Developpement, Université de Bourgogne
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely pathogenicgermlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot 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 Equipe Genetique des Anomalies du Developpement, Université de Bourgogne, SCV005395952.1

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

Last Updated: Nov 18, 2024