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NM_001379451.1(BCORL1):c.26G>A (p.Ser9Asn) AND Shukla-Vernon syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 9, 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:
RCV001290427.2

Allele description [Variation Report for NM_001379451.1(BCORL1):c.26G>A (p.Ser9Asn)]

NM_001379451.1(BCORL1):c.26G>A (p.Ser9Asn)

Gene:
BCORL1:BCL6 corepressor like 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xq26.1
Genomic location:
Preferred name:
NM_001379451.1(BCORL1):c.26G>A (p.Ser9Asn)
HGVS:
  • NC_000023.11:g.130005257G>A
  • NG_021274.1:g.27565G>A
  • NM_001184772.3:c.26G>A
  • NM_001379450.1:c.26G>A
  • NM_001379451.1:c.26G>AMANE SELECT
  • NM_021946.5:c.26G>A
  • NP_001171701.1:p.Ser9Asn
  • NP_001366379.1:p.Ser9Asn
  • NP_001366380.1:p.Ser9Asn
  • NP_068765.3:p.Ser9Asn
  • LRG_628t1:c.26G>A
  • LRG_628:g.27565G>A
  • NC_000023.10:g.129139233G>A
  • NM_021946.4:c.26G>A
Protein change:
S9N
Links:
dbSNP: rs1928393361
NCBI 1000 Genomes Browser:
rs1928393361
Molecular consequence:
  • NM_001184772.3:c.26G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001379450.1:c.26G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001379451.1:c.26G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_021946.5:c.26G>A - missense variant - [Sequence Ontology: SO:0001583]
Observations:
1

Condition(s)

Name:
Shukla-Vernon syndrome
Identifiers:
MONDO: MONDO:0026727; MedGen: C5193146; OMIM: 301029

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001478455Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Feb 9, 2021) 		maternalclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedmaternalyes1not 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 for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen, SCV001478455.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
11not providednot providedclinical testing PubMed (1)

Description

The variant has not yet been reported in the relevant databases (dbSNP151, gnomAD, ClinVar) or in the literature. From a bioinformatics point of view, the change is classified as "likely disease causing" (PolyPhen2, Mutation Taster, SIFT). At this point in time, the variant is to be regarded as a "variant of uncertain clinical significance" (ACMG criteria).

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

Last Updated: Jul 26, 2022