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NM_001042492.3(NF1):c.889-11_889-6delinsAAATT AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Jan 1, 2022
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:
RCV002495882.1

Allele description [Variation Report for NM_001042492.3(NF1):c.889-11_889-6delinsAAATT]

NM_001042492.3(NF1):c.889-11_889-6delinsAAATT

Gene:
NF1:neurofibromin 1 [Gene - OMIM - HGNC]
Variant type:
Indel
Cytogenetic location:
17q11.2
Genomic location:
Preferred name:
NM_001042492.3(NF1):c.889-11_889-6delinsAAATT
HGVS:
  • NC_000017.11:g.31200411_31200416delinsAAATT
  • NG_009018.1:g.110435_110440delinsAAATT
  • NM_000267.3:c.889-11_889-6delinsAAATT
  • NM_001042492.3:c.889-11_889-6delinsAAATTMANE SELECT
  • NM_001128147.3:c.889-11_889-6delinsAAATT
  • LRG_214t1:c.889-11_889-6delinsAAATT
  • LRG_214:g.110435_110440delinsAAATT
  • NC_000017.10:g.29527429_29527434delinsAAATT
Links:
dbSNP: rs2143871690
NCBI 1000 Genomes Browser:
rs2143871690
Molecular consequence:
  • NM_000267.3:c.889-11_889-6delinsAAATT - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001042492.3:c.889-11_889-6delinsAAATT - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001128147.3:c.889-11_889-6delinsAAATT - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Neurofibromatosis, familial spinal (FSNF)
Identifiers:
MONDO: MONDO:0008078; MedGen: C1834235; Orphanet: 636; OMIM: 162210
Name:
Juvenile myelomonocytic leukemia (JMML)
Synonyms:
LEUKEMIA, JUVENILE MYELOMONOCYTIC, SOMATIC
Identifiers:
MONDO: MONDO:0011908; MedGen: C0349639; Orphanet: 86834; OMIM: 607785; Human Phenotype Ontology: HP:0012209
Name:
Neurofibromatosis, type 1 (NF1)
Synonyms:
NEUROFIBROMATOSIS, TYPE I; Recklinghausen's disease; Von Recklinghausen disease; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0018975; MedGen: C0027831; Orphanet: 636; OMIM: 162200
Name:
Neurofibromatosis-Noonan syndrome (NFNS)
Synonyms:
Neurofibromatosis with Noonan phenotype
Identifiers:
MONDO: MONDO:0011035; MedGen: C2931482; Orphanet: 638; OMIM: 601321
Name:
Café-au-lait macules with pulmonary stenosis (WTSN)
Synonyms:
Pulmonic stenosis with cafe-au-lait spots
Identifiers:
MONDO: MONDO:0008672; MedGen: C0553586; OMIM: 193520

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002777413Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Jan 1, 2022) 		unknownclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot 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 Fulgent Genetics, Fulgent Genetics, SCV002777413.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 1, 2024