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NM_000368.4(TSC1):c.-234-1616_-234-235del1382 AND Tuberous sclerosis 1

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 5, 2019
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:
RCV001058317.10

Allele description [Variation Report for NM_000368.4(TSC1):c.-234-1616_-234-235del1382]

NM_000368.4(TSC1):c.-234-1616_-234-235del1382

Genes:
TSC1:TSC complex subunit 1 [Gene - OMIM - HGNC]
GFI1B:growth factor independent 1B transcriptional repressor [Gene - OMIM - HGNC]
MIR548AW:microRNA 548aw [Gene - HGNC]
Variant type:
Deletion
Cytogenetic location:
9q34.13
Genomic location:
Preferred name:
NM_000368.4(TSC1):c.-234-1616_-234-235del1382
HGVS:
  • NC_000009.12:g.132944870_132946251del
  • NG_012386.1:g.3385_4766del
  • NG_034227.1:g.4326_5707del
  • NG_117955.1:g.483_934del
  • NG_117955.2:g.483_1046del
  • LRG_486t1:c.-234-1616_-234-235del1382
  • LRG_486:g.3385_4766del
  • LRG_879:g.4326_5707del
  • NC_000009.11:g.135820255_135821636del
  • NC_000009.11:g.135820257_135821638del
  • NM_000368.4:c.-234-1616_-234-235del1382
Links:

Condition(s)

Name:
Tuberous sclerosis 1 (TSC1)
Identifiers:
MONDO: MONDO:0008612; MedGen: C1854465; Orphanet: 805; OMIM: 191100

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001222877Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(Nov 5, 2019) 		germlineclinical testing

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

Help

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 Labcorp Genetics (formerly Invitae), Labcorp, SCV001222877.3

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

Description

This variant occurs in a non-coding region of the TSC1 gene. It does not change the encoded amino acid sequence of the TSC1 protein. This variant has not been reported in the literature in individuals with TSC1-related conditions. Experimental studies and prediction algorithms are not available for this variant, and the functional significance of this non-coding change is currently unknown. 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: Nov 3, 2024