NM_000268.4(NF2):c.810+2T>C AND Neurofibromatosis, type 2

Clinical significance:Pathogenic (Last evaluated: May 28, 2019)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000990413.1

Allele description [Variation Report for NM_000268.4(NF2):c.810+2T>C]

NM_000268.4(NF2):c.810+2T>C

Gene:
NF2:NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q12.2
Genomic location:
Preferred name:
NM_000268.4(NF2):c.810+2T>C
HGVS:
  • NC_000022.11:g.29661341T>C
  • NG_009057.1:g.62786T>C
  • NM_000268.4:c.810+2T>CMANE SELECT
  • NM_016418.5:c.810+2T>C
  • NM_181825.3:c.810+2T>C
  • NM_181828.3:c.684+2T>C
  • NM_181829.3:c.687+2T>C
  • NM_181830.3:c.561+2T>C
  • NM_181831.3:c.561+2T>C
  • NM_181832.3:c.810+2T>C
  • NM_181833.3:c.447+19056T>C
  • LRG_511t2:c.810+2T>C
  • LRG_511:g.62786T>C
  • NC_000022.10:g.30057330T>C
Links:
dbSNP: rs1601624296
NCBI 1000 Genomes Browser:
rs1601624296
Molecular consequence:
  • NM_181833.3:c.447+19056T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_000268.4:c.810+2T>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_016418.5:c.810+2T>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181825.3:c.810+2T>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181828.3:c.684+2T>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181829.3:c.687+2T>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181830.3:c.561+2T>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181831.3:c.561+2T>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_181832.3:c.810+2T>C - splice donor variant - [Sequence Ontology: SO:0001575]

Condition(s)

Name:
Neurofibromatosis, type 2 (NF2)
Synonyms:
NF 2; Neurofibromatosis central type; Acoustic schwannomas bilateral; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0007039; MedGen: C0027832; Orphanet: 637; OMIM: 101000

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001141393Mendelicscriteria provided, single submitter
Pathogenic
(May 28, 2019)
unknownclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Mendelics, SCV001141393.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 30, 2021

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