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NM_000487.6(ARSA):c.684+33C>T AND Metachromatic leukodystrophy

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jun 15, 2021
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:
RCV001527488.1

Allele description [Variation Report for NM_000487.6(ARSA):c.684+33C>T]

NM_000487.6(ARSA):c.684+33C>T

Gene:
ARSA:arylsulfatase A [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q13.33
Genomic location:
Preferred name:
NM_000487.6(ARSA):c.684+33C>T
HGVS:
  • NC_000022.11:g.50626801G>A
  • NG_009260.2:g.6379C>T
  • NM_000487.6:c.684+33C>TMANE SELECT
  • NM_001085425.3:c.684+33C>T
  • NM_001085426.3:c.684+33C>T
  • NM_001085427.3:c.684+33C>T
  • NM_001085428.3:c.426+33C>T
  • NM_001362782.2:c.426+33C>T
  • NC_000022.10:g.51065229G>A
Links:
dbSNP: rs6151416
NCBI 1000 Genomes Browser:
rs6151416
Molecular consequence:
  • NM_000487.6:c.684+33C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001085425.3:c.684+33C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001085426.3:c.684+33C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001085427.3:c.684+33C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001085428.3:c.426+33C>T - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001362782.2:c.426+33C>T - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Metachromatic leukodystrophy (MLD)
Synonyms:
Metachromatic leukoencephalopathy; Sulfatide lipidosis; Cerebral sclerosis diffuse metachromatic form; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0018868; MedGen: C0023522; Orphanet: 512; OMIM: 250100

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001738518Pars Genome Lab
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely benign
(Jun 15, 2021) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenonot 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 Pars Genome Lab, SCV001738518.1

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

Last Updated: Sep 29, 2024