NM_001370259.2(MEN1):c.783+1G>A AND not specified

Clinical significance:Pathogenic (Last evaluated: Feb 5, 2017)

Review status:1 star out of maximum of 4 stars

criteria provided, single submitter

Based on:
1 submission [Details]
Record status:
current
Accession:
RCV000506752.2

Allele description [Variation Report for NM_001370259.2(MEN1):c.783+1G>A]

NM_001370259.2(MEN1):c.783+1G>A

Gene:
MEN1:menin 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11q13.1
Genomic location:
Preferred name:
NM_001370259.2(MEN1):c.783+1G>A
HGVS:
  • NC_000011.10:g.64807551C>T
  • NG_008929.1:g.8744G>A
  • NG_033040.1:g.691G>A
  • NM_000244.3:c.798+1G>A
  • NM_001370251.1:c.783+1G>A
  • NM_001370259.2:c.783+1G>AMANE SELECT
  • NM_001370260.1:c.783+1G>A
  • NM_001370261.1:c.783+1G>A
  • NM_001370262.1:c.678+1G>A
  • NM_001370263.1:c.678+1G>A
  • NM_130799.2:c.783+1G>A
  • NM_130800.2:c.798+1G>A
  • NM_130801.2:c.798+1G>A
  • NM_130802.2:c.798+1G>A
  • NM_130803.2:c.798+1G>A
  • NM_130804.2:c.798+1G>A
  • LRG_509t1:c.798+1G>A
  • LRG_509t2:c.783+1G>A
  • LRG_509:g.8744G>A
  • NC_000011.9:g.64575023C>T
Links:
dbSNP: rs794728652
NCBI 1000 Genomes Browser:
rs794728652
Molecular consequence:
  • NM_000244.3:c.798+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001370251.1:c.783+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001370259.2:c.783+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001370260.1:c.783+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001370261.1:c.783+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001370262.1:c.678+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001370263.1:c.678+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_130799.2:c.783+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_130800.2:c.798+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_130801.2:c.798+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_130802.2:c.798+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_130803.2:c.798+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_130804.2:c.798+1G>A - splice donor variant - [Sequence Ontology: SO:0001575]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000604214ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratoriescriteria provided, single submitter
Pathogenic
(Feb 5, 2017)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories, SCV000604214.1

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

Last Updated: Nov 11, 2021

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