Is TSC2 p.Val692Phe (c.2074G>T) pathogenic?

TSC2 p.Val692Phe (c.2074G>T) is classified Uncertain significance in TSC2 (ClinVar, Single submitter, 1 submitter; last evaluated 2020-01-05). AlphaMissense: ambiguous (0.4347); Absent from gnomAD v4.1; Associated with tuberous sclerosis 2.

What condition is associated with TSC2 p.Val692Phe (c.2074G>T)?

TSC2 p.Val692Phe (c.2074G>T) is associated with tuberous sclerosis 2 (ClinVar).

How common is TSC2 p.Val692Phe (c.2074G>T) in the general population?

TSC2 p.Val692Phe (c.2074G>T) is absent from gnomAD v4.1 (gnomAD).

How is Tuberous sclerosis complex inherited?

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

What do computational predictors say about TSC2 p.Val692Phe (c.2074G>T)?

AlphaMissense predicts ambiguous (score 0.4347) — an in-silico prediction, not a clinical call.

TSC2 p.Val692Phe

c.2074G>T · rs201769220 · VCV406002

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.4347 · ACMG-weighted

gnomAD v4.1

Not reported

no allele count reported in gnomAD v4.1 (AN 1,592,924)

Missense predictors

1/2 damaging

REVEL, SaProt · AlphaMissense no call

Conditions

tuberous sclerosis 2

Computational evidence

Protein change
AlphaMissense	0.4347	ambiguous
REVEL	0.876	moderately pathogenic-leaning
SaProt	LLR -6.05	tolerated
⇒ REVEL calls this damaging; SaProt does not; AlphaMissense makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 8.4	GERP 1, phastCons 1
Regional constraint	o/e 1.00	unconstrained · MANE · 37 kb · p 0.88 · regional, not allelic
Overall
CADD	23.1	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

Population frequency

gnomAD v4.1 · exomes + genomes

No allele count reported in gnomAD v4.1 (AN 1,592,924). This is missing data, not an absence: the variant may or may not be present in gnomAD. Rarity (ACMG PM2) and BA1/BS1 cannot be assessed for it.

Variant & gene context

Gene: TSC2
Protein: p.Val692Phe
Coding: c.2074G>T
MANE Select: NM_000548
dbSNP: rs201769220
Type: single nucleotide variant
Location: chr16:2071911 (GRCh38)
Gene constraint: LOEUF 0.203 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 68.81 · 2 PDB
Residue 692: an α-helix

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

Disease context

tuberous sclerosis 2 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Tuberous sclerosis complex (Orphanet):

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

Similar variants

TSC2 p.Val692= Likely benign ★★ same residue
TSC2 p.Val692Ala Uncertain significance ★ ⚠ same residue
TSC2 p.Val692Ile Conflicting classifications of pathogenicity ★ ⚠ same residue
TSC2 p.Val692Leu Uncertain significance ★ ⚠ same residue
TSC2 p.Val692_Leu693insVal 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

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-val692phe (accessed [today's date]).

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