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NM_000543.5(SMPD1):c.996dup (p.Phe333fs) AND multiple conditions

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Dec 30, 2020
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:
RCV001281410.1

Allele description [Variation Report for NM_000543.5(SMPD1):c.996dup (p.Phe333fs)]

NM_000543.5(SMPD1):c.996dup (p.Phe333fs)

Gene:
SMPD1:sphingomyelin phosphodiesterase 1 [Gene - OMIM - HGNC]
Variant type:
Duplication
Cytogenetic location:
11p15.4
Genomic location:
Preferred name:
NM_000543.5(SMPD1):c.996dup (p.Phe333fs)
HGVS:
  • NC_000011.10:g.6392061dup
  • NG_011780.1:g.6637dup
  • NM_000543.5:c.996dupMANE SELECT
  • NM_001007593.3:c.993dup
  • NM_001318087.2:c.996dup
  • NM_001318088.2:c.35dup
  • NM_001365135.2:c.996dup
  • NP_000534.3:p.Phe333fs
  • NP_001007594.2:p.Phe332fs
  • NP_001305016.1:p.Phe333fs
  • NP_001305017.1:p.Ser13fs
  • NP_001352064.1:p.Phe333fs
  • NC_000011.9:g.6413291dup
  • NM_000543.4:c.996dupC
  • NR_027400.3:n.1121dup
Protein change:
F332fs
Links:
dbSNP: rs387906289
NCBI 1000 Genomes Browser:
rs387906289
Molecular consequence:
  • NM_000543.5:c.996dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001007593.3:c.993dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001318087.2:c.996dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001318088.2:c.35dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NM_001365135.2:c.996dup - frameshift variant - [Sequence Ontology: SO:0001589]
  • NR_027400.3:n.1121dup - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Niemann-Pick disease, type B
Identifiers:
MONDO: MONDO:0011871; MedGen: C0268243; Orphanet: 77293; OMIM: 607616
Name:
Niemann-Pick disease, type A
Synonyms:
SPHINGOMYELIN LIPIDOSIS; SPHINGOMYELINASE DEFICIENCY
Identifiers:
MONDO: MONDO:0009756; MedGen: C0268242; Orphanet: 77292; OMIM: 257200

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001468715Huiwen Zhang's lab, Shanghai Jiao Tong University School of Medicine, Xinhua Hospital
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(Dec 30, 2020) 		inheritedclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedinheritedyesnot 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 Huiwen Zhang's lab, Shanghai Jiao Tong University School of Medicine, Xinhua Hospital, SCV001468715.1

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

Last Updated: Jul 29, 2023