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NM_021096.4(CACNA1I):c.3392G>T (p.Arg1131Leu) AND Neurodevelopmental disorder with speech impairment and with or without seizures

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 2, 2024
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:
RCV004587481.1

Allele description [Variation Report for NM_021096.4(CACNA1I):c.3392G>T (p.Arg1131Leu)]

NM_021096.4(CACNA1I):c.3392G>T (p.Arg1131Leu)

Gene:
CACNA1I:calcium voltage-gated channel subunit alpha1 I [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q13.1
Genomic location:
Preferred name:
NM_021096.4(CACNA1I):c.3392G>T (p.Arg1131Leu)
HGVS:
  • NC_000022.11:g.39662795G>T
  • NG_052947.1:g.97043G>T
  • NM_001003406.2:c.3287G>T
  • NM_021096.4:c.3392G>TMANE SELECT
  • NP_001003406.1:p.Arg1096Leu
  • NP_066919.2:p.Arg1131Leu
  • NC_000022.10:g.40058800G>T
  • NM_021096.3:c.3392G>T
Protein change:
R1096L
Molecular consequence:
  • NM_001003406.2:c.3287G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_021096.4:c.3392G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Neurodevelopmental disorder with speech impairment and with or without seizures
Synonyms:
Neurodevelopmental disorder with variable intellectual disability and speech impairment, with or without seizures
Identifiers:
MONDO: MONDO:0859313; MedGen: C5774252; OMIM: 620114

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005077703Institute of Immunology and Genetics Kaiserslautern
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(May 2, 2024) 		germlineclinical 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 Institute of Immunology and Genetics Kaiserslautern, SCV005077703.1

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

Description

ACMG Criteria: PM2, PP3; Variant was found in heterozygous state

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

Last Updated: Nov 3, 2024