NM_001170629.2(CHD8):c.262G>A (p.Glu88Lys) AND History of neurodevelopmental disorder

Clinical significance:Likely benign (Last evaluated: Jul 24, 2018)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000719985.1

Allele description [Variation Report for NM_001170629.2(CHD8):c.262G>A (p.Glu88Lys)]

NM_001170629.2(CHD8):c.262G>A (p.Glu88Lys)

Gene:
CHD8:chromodomain helicase DNA binding protein 8 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
14q11.2
Genomic location:
Preferred name:
NM_001170629.2(CHD8):c.262G>A (p.Glu88Lys)
HGVS:
  • NC_000014.9:g.21431382C>T
  • NG_021249.1:g.10917G>A
  • NM_001170629.2:c.262G>AMANE SELECT
  • NM_020920.4:c.6+429G>A
  • NP_001164100.1:p.Glu88Lys
  • NP_001164100.1:p.Glu88Lys
  • NC_000014.8:g.21899541C>T
  • NM_001170629.1:c.262G>A
Protein change:
E88K
Links:
dbSNP: rs78640816
NCBI 1000 Genomes Browser:
rs78640816
Molecular consequence:
  • NM_020920.4:c.6+429G>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001170629.2:c.262G>A - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
History of neurodevelopmental disorder
Identifiers:
MedGen: C2711754

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000850859Ambry Geneticscriteria provided, single submitter
Likely benign
(Jul 24, 2018)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not providednot provided1not providedclinical testing

Details of each submission

From Ambry Genetics, SCV000850859.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided

Description

In silico models in agreement (benign);Subpopulation frequency in support of benign classification

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown1not providednot provided1not providednot providednot provided

Last Updated: Aug 17, 2021

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