U.S. flag

An official website of the United States government

NM_000368.5(TSC1):c.3140C>T (p.Thr1047Ile) AND Tuberous sclerosis syndrome

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 13, 2023
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:
RCV003997360.2

Allele description [Variation Report for NM_000368.5(TSC1):c.3140C>T (p.Thr1047Ile)]

NM_000368.5(TSC1):c.3140C>T (p.Thr1047Ile)

Gene:
TSC1:TSC complex subunit 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q34.13
Genomic location:
Preferred name:
NM_000368.5(TSC1):c.3140C>T (p.Thr1047Ile)
HGVS:
  • NC_000009.12:g.132896590G>A
  • NG_012386.1:g.53044C>T
  • NM_000368.5:c.3140C>TMANE SELECT
  • NM_001162426.2:c.3137C>T
  • NM_001162427.2:c.2987C>T
  • NM_001362177.2:c.2777C>T
  • NP_000359.1:p.Thr1047Ile
  • NP_000359.1:p.Thr1047Ile
  • NP_001155898.1:p.Thr1046Ile
  • NP_001155899.1:p.Thr996Ile
  • NP_001349106.1:p.Thr926Ile
  • LRG_486t1:c.3140C>T
  • LRG_486:g.53044C>T
  • LRG_486p1:p.Thr1047Ile
  • NC_000009.11:g.135771977G>A
  • NM_000368.4:c.3140C>T
Protein change:
T1046I
Links:
dbSNP: rs587778726
NCBI 1000 Genomes Browser:
rs587778726
Molecular consequence:
  • NM_000368.5:c.3140C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001162426.2:c.3137C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001162427.2:c.2987C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001362177.2:c.2777C>T - missense variant - [Sequence Ontology: SO:0001583]
Observations:
3

Condition(s)

Name:
Tuberous sclerosis syndrome (TSC)
Synonyms:
Tuberous sclerosis
Identifiers:
MONDO: MONDO:0001734; MedGen: C0041341; OMIM: PS191100

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004829463All of Us Research Program, National Institutes of Health
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain Significance
(Dec 13, 2023) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknown3not providednot provided108544not 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 All of Us Research Program, National Institutes of Health, SCV004829463.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided3not providednot providedclinical testing PubMed (1)

Description

This missense variant replaces threonine with isoleucine at codon 1047 of the TSC1 protein. Computational prediction suggests that this variant may not impact protein structure and function (internally defined REVEL score threshold <= 0.5, PMID: 27666373). To our knowledge, functional studies have not been reported for this variant. This variant has not been reported in individuals affected with TSC1-related disorders in the literature. This variant has been identified in 2/282234 chromosomes in the general population by the Genome Aggregation Database (gnomAD). The available evidence is insufficient to determine the role of this variant in disease conclusively. Therefore, this variant is classified as a Variant of Uncertain Significance.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknown108544not providednot provided3not providednot providednot provided

Last Updated: Jun 2, 2024