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NM_152564.5(VPS13B):c.1121C>T (p.Thr374Ile) AND Cohen syndrome

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Sep 13, 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:
RCV001279381.5

Allele description [Variation Report for NM_152564.5(VPS13B):c.1121C>T (p.Thr374Ile)]

NM_152564.5(VPS13B):c.1121C>T (p.Thr374Ile)

Gene:
VPS13B:vacuolar protein sorting 13 homolog B [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
8q22.2
Genomic location:
Preferred name:
NM_152564.5(VPS13B):c.1121C>T (p.Thr374Ile)
HGVS:
  • NC_000008.11:g.99121360C>T
  • NG_007098.2:g.113095C>T
  • NM_015243.3:c.1121C>T
  • NM_017890.5:c.1121C>T
  • NM_152564.5:c.1121C>TMANE SELECT
  • NM_181661.3:c.1121C>T
  • NP_056058.2:p.Thr374Ile
  • NP_060360.3:p.Thr374Ile
  • NP_689777.3:p.Thr374Ile
  • NP_858047.2:p.Thr374Ile
  • LRG_351t1:c.1121C>T
  • LRG_351:g.113095C>T
  • NC_000008.10:g.100133588C>T
  • NM_017890.4:c.1121C>T
  • NR_047582.2:n.1339C>T
Protein change:
T374I
Links:
dbSNP: rs753781360
NCBI 1000 Genomes Browser:
rs753781360
Molecular consequence:
  • NM_015243.3:c.1121C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_017890.5:c.1121C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_152564.5:c.1121C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_181661.3:c.1121C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NR_047582.2:n.1339C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Name:
Cohen syndrome (COH1)
Synonyms:
Pepper syndrome; Cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness
Identifiers:
MONDO: MONDO:0008999; MedGen: C0265223; Orphanet: 193; OMIM: 216550

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001466471Natera, Inc.
no assertion criteria provided
Likely benign
(Sep 23, 2020)
germlineclinical testing

SCV001502724Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Uncertain significance
(Sep 13, 2022)
germlineclinical testing

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

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Natera, Inc., SCV001466471.1

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

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001502724.3

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

Description

This sequence change replaces threonine, which is neutral and polar, with isoleucine, which is neutral and non-polar, at codon 374 of the VPS13B protein (p.Thr374Ile). This variant is present in population databases (rs753781360, gnomAD 0.05%). This variant has not been reported in the literature in individuals affected with VPS13B-related conditions. ClinVar contains an entry for this variant (Variation ID: 991206). Advanced modeling of protein sequence and biophysical properties (such as structural, functional, and spatial information, amino acid conservation, physicochemical variation, residue mobility, and thermodynamic stability) performed at Invitae indicates that this missense variant is not expected to disrupt VPS13B protein function. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

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

Last Updated: Sep 29, 2024