chr16-2084676-C-T

Variant names:

Variant summary

Our verdict is Benign. The variant received -7 ACMG points: 0P and 7B. BP4_ModerateBP6BS2

The NM_000548.5(TSC2):c.4454C>T(p.Thr1485Ile) variant causes a missense change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.00000761 in 1,446,404 control chromosomes in the GnomAD database, with no homozygous occurrence. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Conflicting classifications of pathogenicity (no stars). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. T1485S) has been classified as Uncertain significance.

Frequency

Genomes: not found (cov: 34)

Exomes 𝑓: 0.0000076 ( 0 hom. )

Consequence

TSC2
NM_000548.5 missense

Scores

Clinical Significance

Conflicting classifications of pathogenicity criteria provided, conflicting classifications U:1B:2

Conservation

PhyloP100: 2.90

Publications

1 publications found

Variant links:

Genes affected

TSC2 (HGNC:12363): (TSC complex subunit 2) This gene is a tumor suppressor gene that encodes the growth inhibitory protein tuberin. Tuberin interacts with hamartin to form the TSC protein complex which functions in the control of cell growth. This TSC protein complex negatively regulates mammalian target of rapamycin complex 1 (mTORC1) signaling which is a major regulator of anabolic cell growth. Mutations in this gene have been associated with tuberous sclerosis and lymphangioleiomyomatosis. [provided by RefSeq, May 2022]

TSC2 Gene-Disease associations (from GenCC):

tuberous sclerosis
Inheritance: AD Classification: DEFINITIVE Submitted by: ClinGen
tuberous sclerosis 2
Inheritance: AD Classification: DEFINITIVE, STRONG Submitted by: PanelApp Australia, Laboratory for Molecular Medicine, Labcorp Genetics (formerly Invitae), G2P, Genomics England PanelApp, Ambry Genetics
lymphangioleiomyomatosis
Inheritance: AD Classification: STRONG Submitted by: Genomics England PanelApp
tuberous sclerosis complex
Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet

TSC2 links:

Genome browser will be placed here

ACMG classification

Classification was made for transcript

Our verdict: Benign. The variant received -7 ACMG points.

BP4

Computational evidence support a benign effect (MetaRNN=0.2029993).

BP6

Variant 16-2084676-C-T is Benign according to our data. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928. Variant chr16-2084676-C-T is described in CliVar as Conflicting_classifications_of_pathogenicity. Clinvar id is 535928.

BS2

High AC in GnomAdExome4 at 11 AD gene.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TSC2	NM_000548.5 link	c.4454C>T	p.Thr1485Ile	missense_variant	Exon 34 of 42	ENST00000219476.9	NP_000539.2	P49815-1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TSC2	ENST00000219476.9 link	c.4454C>T	p.Thr1485Ile	missense_variant	Exon 34 of 42	5	NM_000548.5	ENSP00000219476.3		P49815-1

Frequencies

GnomAD3 genomes

Cov.:

GnomAD2 exomes

AF:

0.0000126

AC:

AN:

237482

AF XY:

0.00000769

show subpopulations

Gnomad AFR exome

AF:

0.00

Gnomad AMR exome

AF:

0.00

Gnomad ASJ exome

AF:

0.00

Gnomad EAS exome

AF:

0.00

Gnomad FIN exome

AF:

0.00

Gnomad NFE exome

AF:

0.00

Gnomad OTH exome

AF:

0.000167

GnomAD4 exome

AF:

0.00000761

AC:

AN:

1446404

Hom.:

Cov.:

AF XY:

0.00000556

AC XY:

AN XY:

719970

show subpopulations

African (AFR)

AF:

0.00

AC:

AN:

33472

American (AMR)

AF:

0.00

AC:

AN:

44712

Ashkenazi Jewish (ASJ)

AF:

0.00

AC:

AN:

26130

East Asian (EAS)

AF:

0.00

AC:

AN:

39692

South Asian (SAS)

AF:

0.0000348

AC:

AN:

86258

European-Finnish (FIN)

AF:

0.00

AC:

AN:

38242

Middle Eastern (MID)

AF:

0.00

AC:

AN:

5768

European-Non Finnish (NFE)

AF:

0.00000540

AC:

AN:

1111846

Other (OTH)

AF:

0.0000332

AC:

AN:

60284

Allele Balance Distribution

Red line indicates average allele balance

Average allele balance: 0.484

Heterozygous variant carriers

0.00

0.20

0.40

0.60

0.80

0.95

Allele balance

Age Distribution

Exome Het

Variant carriers

<30

30-35

35-40

40-45

45-50

50-55

55-60

60-65

65-70

70-75

75-80

>80

Age

GnomAD4 genome

Cov.:

Alfa

AF:

0.00

Hom.:

ExAC

AF:

0.0000249

AC:

ClinVar

Significance: Conflicting classifications of pathogenicity

Submissions summary: Uncertain:1Benign:2

Revision: criteria provided, conflicting classifications

LINK: link

Submissions by phenotype

Hereditary cancer-predisposing syndrome

Uncertain:1

Jun 10, 2025

Ambry Genetics

Significance:Uncertain significance

Review Status:criteria provided, single submitter

Collection Method:clinical testing

The p.T1485I variant (also known as c.4454C>T), located in coding exon 33 of the TSC2 gene, results from a C to T substitution at nucleotide position 4454. The threonine at codon 1485 is replaced by isoleucine, an amino acid with similar properties. This amino acid position is conserved. In addition, the in silico prediction for this alteration is inconclusive. Since supporting evidence is limited at this time, the clinical significance of this alteration remains unclear. -

Tuberous sclerosis syndrome

Benign:1

Jul 22, 2023

All of Us Research Program, National Institutes of Health

Significance:Likely benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Tuberous sclerosis 2

Benign:1

Oct 26, 2024

Labcorp Genetics (formerly Invitae), Labcorp

Significance:Benign

Review Status:criteria provided, single submitter

Collection Method:clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

AlphaMissense

Benign

0.12

BayesDel_addAF

Uncertain

0.050

BayesDel_noAF

Uncertain

0.040

CADD

Benign

(source)

DANN

Benign

0.93

DEOGEN2

Uncertain

0.53

D;.;.;.;.;.;.;.;.;.;.;.;T;.;T

Eigen

Benign

-0.59

Eigen_PC

Benign

-0.50

FATHMM_MKL

Benign

0.68

LIST_S2

Uncertain

0.94

D;D;D;D;D;D;D;D;D;D;D;D;D;D;D

M_CAP

Pathogenic

0.35

MetaRNN

Benign

0.20

T;T;T;T;T;T;T;T;T;T;T;T;T;T;T

MetaSVM

Benign

-0.36

MutationAssessor

Benign

0.0

N;.;.;.;.;.;.;.;.;.;.;.;.;.;.

PhyloP100

2.9

PrimateAI

Benign

0.31

PROVEAN

Benign

-1.7

N;.;.;N;.;N;.;.;N;N;.;.;.;.;N

REVEL

Uncertain

0.49

Sift

Benign

0.15

T;.;.;T;.;T;.;.;T;T;.;.;.;.;T

Sift4G

Benign

0.19

T;.;.;T;.;T;.;.;T;T;.;.;.;.;T

Polyphen

0.21

B;.;.;.;B;B;.;.;B;B;.;.;.;.;.

Vest4

0.27

MutPred

0.32

Loss of glycosylation at T1485 (P = 0.0087);.;.;.;.;.;.;Loss of glycosylation at T1485 (P = 0.0087);.;.;.;.;.;.;.;

MVP

0.96

ClinPred

0.085

GERP RS

4.1

Varity_R

0.046

gMVP

0.35

Mutation Taster

=94/6

polymorphism

(source)

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.020

Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

You must be logged in to view publications. This limit was set because tens of millions (!) of queries from AI bots are generated daily.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

Publications

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

Age Distribution

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

Other links and lift over