Is TSC2 p.Ser1095= (c.3285C>T) pathogenic?

TSC2 p.Ser1095= (c.3285C>T) is classified Likely benign in TSC2 (ClinVar, Multiple submitters, 3 submitters; last evaluated 2024-02-24). Very rare (popmax 0.0011%, sas); Associated with tuberous sclerosis.

What condition is associated with TSC2 p.Ser1095= (c.3285C>T)?

TSC2 p.Ser1095= (c.3285C>T) is associated with tuberous sclerosis, tuberous sclerosis 2, hereditary neoplastic syndrome (ClinVar).

How common is TSC2 p.Ser1095= (c.3285C>T) in the general population?

TSC2 p.Ser1095= (c.3285C>T) is very rare (popmax 0.0011%, sas) (gnomAD).

How is Tuberous sclerosis complex inherited?

Typically Autosomal dominant (Orphanet). A genetic counselor can assess individual risk for a family.

TSC2 p.Ser1095=

c.3285C>T · rs745446277 · VCV467998

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 3 submitters

gnomAD v4.1

Rare

very rare (popmax 0.0011%, sas)

Conditions

tuberous sclerosis

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	<0.2	all four deltas below 0.2 · C>G here scores Δ0.35 · evaluated, not missing
Constraint at this position
Conservation	phyloP 1	GERP -1.6, phastCons 0.64
Overall
CADD	6.375	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0011% South Asian · 1/90,512 alleles

Filtering AF 7.9e-05% ClinGen BA1/BS1 input FAF95, joint · FAF99 5.4e-05%

Overall 0.000311% 5/1,609,556 alleles · very rare

Ancestry group	Frequency	1 in
South Asiangrpmax	0.0011%	90,512
European (non-Finnish)	0.000339%	294,664

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene: TSC2
Protein: p.Ser1095=
Coding: c.3285C>T
MANE Select: NM_000548
dbSNP: rs745446277
Type: single nucleotide variant
Location: chr16:2079557 (GRCh38)
Gene constraint: LOEUF 0.203 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 68.81 · 2 PDB
Residue 1095: the 'disordered' region

Full TSC2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

tuberous sclerosis — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: tuberous sclerosis 2 hereditary neoplastic syndrome

For Tuberous sclerosis complex (Orphanet):

Inheritance: Autosomal dominant
Onset: All ages
Prevalence: 1-9 / 100 000 (Taiwan, Province of China)

Similar variants

TSC2 p.Ser1095Asn Pathogenic/Likely pathogenic ★★ ⚠ same residue
TSC2 p.Ser1095Cys Uncertain significance ★★ ⚠ same residue
TSC2 p.Ser1095Gly Uncertain significance ★★ ⚠ same residue
TSC2 p.Ser1095Ile Uncertain significance ★ ⚠ same residue
TSC2 c.1257+1G>A Pathogenic ★★ same condition
TSC2 c.1258-2A>G Pathogenic ★★ same condition
TSC2 c.1361+1G>A Pathogenic/Likely pathogenic ★★ same condition
TSC2 c.1361+1G>T Pathogenic/Likely pathogenic ★★ same condition

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/tsc2-p-ser1095 (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown