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NM_018668.5(VPS33B):c.-8C>T AND not specified

Germline classification:
Benign (2 submissions)
Last evaluated:
Dec 30, 2014
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:
RCV000173466.9

Allele description [Variation Report for NM_018668.5(VPS33B):c.-8C>T]

NM_018668.5(VPS33B):c.-8C>T

Gene:
VPS33B:VPS33B late endosome and lysosome associated [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
15q26.1
Genomic location:
Preferred name:
NM_018668.5(VPS33B):c.-8C>T
HGVS:
  • NC_000015.10:g.91022257G>A
  • NG_012162.1:g.5347C>T
  • NM_001289148.1:c.-8C>T
  • NM_001289149.1:c.-219C>T
  • NM_018668.5:c.-8C>TMANE SELECT
  • LRG_884:g.5347C>T
  • NC_000015.9:g.91565487G>A
  • NM_018668.3:c.-8C>T
Links:
dbSNP: rs11542639
NCBI 1000 Genomes Browser:
rs11542639
Molecular consequence:
  • NM_001289148.1:c.-8C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_001289149.1:c.-219C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
  • NM_018668.5:c.-8C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000224584Eurofins Ntd Llc (ga)
criteria provided, single submitter

(EGL Classification Definitions 2015)		Benign
(Dec 30, 2014) 		germlineclinical testing

Citation Link,

SCV000313245PreventionGenetics, part of Exact Sciences
criteria provided, single submitter

(ACMG Guidelines, 2015)		Benigngermlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown1not 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 Eurofins Ntd Llc (ga), SCV000224584.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot provided1not providednot providednot provided

From PreventionGenetics, part of Exact Sciences, SCV000313245.1

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

Last Updated: Sep 29, 2024