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NM_001385012.1(NBEA):c.7543C>A (p.Leu2515Met) AND Developmental disorder

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 2, 2021
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:
RCV001843825.2

Allele description [Variation Report for NM_001385012.1(NBEA):c.7543C>A (p.Leu2515Met)]

NM_001385012.1(NBEA):c.7543C>A (p.Leu2515Met)

Gene:
NBEA:neurobeachin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
13q13.3
Genomic location:
Preferred name:
NM_001385012.1(NBEA):c.7543C>A (p.Leu2515Met)
HGVS:
  • NC_000013.11:g.35628174C>A
  • NG_028156.1:g.690888C>A
  • NM_001204197.3:c.922C>A
  • NM_001379245.1:c.7534C>A
  • NM_001385012.1:c.7543C>AMANE SELECT
  • NM_015678.5:c.7543C>A
  • NP_001191126.1:p.Leu308Met
  • NP_001366174.1:p.Leu2512Met
  • NP_001371941.1:p.Leu2515Met
  • NP_056493.3:p.Leu2515Met
  • LRG_602t1:c.7543C>A
  • LRG_602t2:c.922C>A
  • LRG_602t3:c.7543C>A
  • LRG_602:g.690888C>A
  • LRG_602p1:p.Leu2515Met
  • LRG_602p2:p.Leu308Met
  • LRG_602p3:p.Leu2515Met
  • NC_000013.10:g.36202311C>A
  • NM_015678.4:c.7543C>A
Protein change:
L2512M
Links:
dbSNP: rs2153065630
NCBI 1000 Genomes Browser:
rs2153065630
Molecular consequence:
  • NM_001204197.3:c.922C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001379245.1:c.7534C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001385012.1:c.7543C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_015678.5:c.7543C>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Developmental disorder
Identifiers:
MedGen: C0008073

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002102976Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Aug 2, 2021) 		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 Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine, SCV002102976.2

#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: Apr 13, 2025