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NM_000543.5(SMPD1):c.1054G>T (p.Glu352Ter) AND multiple conditions

Germline classification:
Pathogenic (2 submissions)
Last evaluated:
Nov 21, 2023
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV000805997.8

Allele description [Variation Report for NM_000543.5(SMPD1):c.1054G>T (p.Glu352Ter)]

NM_000543.5(SMPD1):c.1054G>T (p.Glu352Ter)

Gene:
SMPD1:sphingomyelin phosphodiesterase 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11p15.4
Genomic location:
Preferred name:
NM_000543.5(SMPD1):c.1054G>T (p.Glu352Ter)
HGVS:
  • NC_000011.10:g.6392119G>T
  • NG_011780.1:g.6695G>T
  • NM_000543.5:c.1054G>TMANE SELECT
  • NM_001007593.3:c.1051G>T
  • NM_001318087.2:c.1054G>T
  • NM_001318088.2:c.93G>T
  • NM_001365135.2:c.1054G>T
  • NP_000534.3:p.Glu352Ter
  • NP_001007594.2:p.Glu351Ter
  • NP_001305016.1:p.Glu352Ter
  • NP_001305017.1:p.Gly31=
  • NP_001352064.1:p.Glu352Ter
  • NC_000011.9:g.6413349G>T
  • NM_000543.4:c.1054G>T
  • NR_027400.3:n.1179G>T
Protein change:
E351*
Links:
dbSNP: rs201550531
NCBI 1000 Genomes Browser:
rs201550531
Molecular consequence:
  • NR_027400.3:n.1179G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_000543.5:c.1054G>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001007593.3:c.1051G>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001318087.2:c.1054G>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001365135.2:c.1054G>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001318088.2:c.93G>T - synonymous variant - [Sequence Ontology: SO:0001819]

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
SCV000945975Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Pathogenic
(Nov 21, 2023) 		germlineclinical testing

PubMed (3)
[See all records that cite these PMIDs]

SCV002796210Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Pathogenic
(Jan 31, 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
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

The demographics and distribution of type B Niemann-Pick disease: novel mutations lead to new genotype/phenotype correlations.

Simonaro CM, Desnick RJ, McGovern MM, Wasserstein MP, Schuchman EH.

Am J Hum Genet. 2002 Dec;71(6):1413-9. Epub 2002 Oct 4.

PubMed [citation]
PMID:
12369017
PMCID:
PMC378582

Screening of 25 Italian patients with Niemann-Pick A reveals fourteen new mutations, one common and thirteen private, in SMPD1.

Ricci V, Stroppiano M, Corsolini F, Di Rocco M, Parenti G, Regis S, Grossi S, Biancheri R, Mazzotti R, Filocamo M.

Hum Mutat. 2004 Jul;24(1):105.

PubMed [citation]
PMID:
15221801
See all PubMed Citations (4)

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV000945975.6

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (3)

Description

This sequence change creates a premature translational stop signal (p.Glu352*) in the SMPD1 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in SMPD1 are known to be pathogenic (PMID: 12369017, 15221801). This variant is present in population databases (rs201550531, gnomAD 0.003%). This variant has not been reported in the literature in individuals affected with SMPD1-related conditions. ClinVar contains an entry for this variant (Variation ID: 650777). Algorithms developed to predict the effect of sequence changes on RNA splicing suggest that this variant may disrupt the consensus splice site. For these reasons, this variant has been classified as Pathogenic.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From Fulgent Genetics, Fulgent Genetics, SCV002796210.1

#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 29, 2024