# NM_001242896.3(DEPDC5):c.1290C>T (p.Pro430=)

https://sugi.bio/variant/depdc5-p-pro430

## Summary

**DEPDC5 p.Pro430= (c.1290C>T)** is classified **Likely benign** in DEPDC5 (ClinVar, Multiple submitters, 5 submitters; last evaluated 2026-01-23). Ultra-rare (popmax 0.0681%, nfe); Associated with familial focal epilepsy with variable foci.

**At a glance:** Likely benign · review: Multiple submitters · rsID rs201202102 · 5 submitters · 1 linked condition · ultra-rare (popmax 0.0681%, nfe)

## For patients & families {#patients}

This is a change in the DEPDC5 gene that is classified as likely benign — not considered disease-causing, submitted by 5 submitters, and is linked to familial focal epilepsy with variable foci.

*Reference information, not medical advice, and not a prediction for any individual. A genetic counselor or clinician can interpret what it means for you and your family.*

|  |  |
| --- | --- |
| Typical inheritance (of this condition) | Autosomal dominant |
| Age of onset (of this condition) | Adolescent, Adult, Childhood, Infancy |
| Diagnostic panels | DEPDC5 is a diagnostic-grade gene on 10 Genomics England panels |

**Commonly reported features of Familial focal epilepsy with variable foci** (across patients with this condition; presentation varies — frequencies from Orphanet):

- Focal-onset seizure — Very frequent (99-80%)
- EEG with focal epileptiform discharges — Very frequent (99-80%)
- Bilateral tonic-clonic seizure — Frequent (79-30%)
- Interictal EEG abnormality — Frequent (79-30%)
- Nocturnal seizures — Frequent (79-30%)
- Atypical behavior — Occasional (29-5%)
- Autistic behavior — Occasional (29-5%)
- Pallor — Occasional (29-5%)

**Support & next steps:** [Condition overview & support (NIH GARD)](https://rarediseases.info.nih.gov/diseases/0013295/index) · [Find a genetic counselor (NSGC)](https://findageneticcounselor.nsgc.org/).

## Identity {#identity}

| Field | Value |
| --- | --- |
| Gene | [DEPDC5](https://sugi.bio/atlas/gene/DEPDC5/) |
| Protein change (HGVS p.) | p.Pro430= |
| Coding change (HGVS c.) | c.1290C>T |
| MANE Select transcript | [NM_001242896](https://www.ncbi.nlm.nih.gov/nuccore/NM_001242896) |
| dbSNP | [rs201202102](https://www.ncbi.nlm.nih.gov/snp/rs201202102/) |
| Variant type | single nucleotide variant |
| Location | chr22:31809613-31809613 (GRCh38) |
| ClinVar | [VCV444584](https://www.ncbi.nlm.nih.gov/clinvar/variation/444584/) |

**All HGVS expressions:** `NC_000022.10:g.32205599C>T`, `NC_000022.11:g.31809613C>T`, `NG_034067.1:g.60663C>T`, `NM_001007188.4:c.1290C>T`, `NM_001136029.4:c.1290C>T`, `NM_001242896.3:c.1290C>T`, `NM_001242897.2:c.1290C>T`, `NM_001363852.2:c.1290C>T`, `NM_001363854.2:c.1290C>T`, `NM_001364318.2:c.1290C>T`, `NM_001364319.2:c.1290C>T`, `NM_001364320.2:c.1290C>T`, `NM_001369901.1:c.1206C>T`, `NM_001369902.1:c.1206C>T`, `NM_001369903.1:c.1290C>T`, `NM_014662.6:c.1290C>T`, `NR_110988.2:n.1496C>T`, `NR_146296.2:n.1379C>T`, `NR_157125.2:n.1375C>T`, `NR_157126.2:n.1379C>T`, `NR_157128.1:n.1496C>T`

## Computational & population evidence {#evidence}

**Concordance:** Mixed / partial computational evidence (see below).

- **Missense predictors (AlphaMissense/REVEL/SaProt) do not apply** to this variant type — they score amino-acid substitutions only. For non-missense variants the computational signal comes from conservation (below), not from a missing predictor score.
- Conservation: phyloP -0.002, GERP 1.42, phastCons 0.947 — not a conserved position (phyloP < 0.1, ACGS BP7 cut)
- CADD: **PHRED 13.53**. No single ClinGen-calibrated threshold exists and the expert panels that use CADD disagree — GUCY2D/AIPL1 require ≥ 20.0 for an untranslated-region variant, ABCA4 ≥ 28.1 for a synonymous or indel variant, the Pulmonary Hypertension panel imports Pejaver 2022's missense-calibrated numbers, and the Antibody Deficiencies panel declines CADD entirely for PIK3CD. CADD v1.7 also incorporates Zoonomia phyloP, so it partly re-expresses the conservation above. *Descriptive; no threshold applied.*
- SpliceAI: **below the reporting threshold**. This position is scored for a different substitution (C>A, Δ0.38 acceptor gain), so this allele was evaluated and its deltas all fell under Δ0.2 — a prediction of no splicing effect for this allele, not a gap in our data. *No ACMG code assigned.*
- Population frequency (gnomAD v4.1): grpmax **0.0681%** (nfe) · FAF95 0.0642% · FAF99 0.0626% · 804/1,179,842 in the highest group · 840/1,613,692 alleles overall — ultra-rare (popmax 0.0681%, nfe).

| Ancestry group | Allele frequency | 1 in |
| --- | --- | --- |
| European (non-Finnish) (grpmax) | 0.0681% | 1,467 |
| Remaining individuals (not grpmax-eligible) | 0.032% | 3,124 |
| Middle Eastern | 0.0164% | 6,082 |
| African / African-American | 0.012% | 8,320 |
| Admixed American | 0.00834% | 11,992 |
| Ashkenazi Jewish (not grpmax-eligible) | 0.00338% | 29,594 |

*Computational predictors are not independent (ClinGen Variant Classification guidance): AlphaMissense (Cheng et al. 2023) carries the ACMG weight for missense and conservation (phyloP/GERP/phastCons) for non-missense; REVEL (Pejaver-2022 calibrated strength bands) and SaProt (Su et al. 2023, structure-aware, ClinVar-independent protein language model, raw LLR) are shown as orthogonal agreement signals, not additive. For frequency, the gnomAD v4.1 grpmax filtering allele frequency (FAF95) is ClinGen's designated BA1/BS1 input (gnomAD v4 guidance v3.0, June 2025); BA1/BS1 thresholds are disease-specific, not a blanket 5%. Predictions, not a clinical determination.*

## Gene constraint & dosage {#gene-context}

**DEPDC5** population constraint: LOEUF 0.403, pLI 1, missense-Z 3.7429; ClinGen dosage — haploinsufficiency 3, triplosensitivity 0 (0–3 scale). *Lower LOEUF and higher pLI indicate a gene that tolerates loss-of-function poorly; ClinGen dosage is the curated haploinsufficiency call.*

Curated gene–disease validity (ClinGen):

- **focal epilepsy** — Definitive (AD)

## Protein context {#protein}

Residue **430** lies in the 'disordered' region.

AlphaFold model confidence (whole protein): pLDDT 65.22, 19% of residues very-high.

**11 experimental structure(s)** (PDB): [6CES](https://www.rcsb.org/structure/6CES), [6CET](https://www.rcsb.org/structure/6CET), [7T3A](https://www.rcsb.org/structure/7T3A), [7T3B](https://www.rcsb.org/structure/7T3B), [7T3C](https://www.rcsb.org/structure/7T3C), [8FW5](https://www.rcsb.org/structure/8FW5).

## What this gene does {#gene-function}

*Describes the biological roles of DEPDC5 (the gene this variant disrupts) — not effects measured for this specific variant. A damaging variant is expected to affect these functions and pathways; the degree depends on the variant.*

**How this variant is thought to act:** DEPDC5's established molecular role includes small GTPase binding. p.Pro430= falls in the disordered region.


### Pathways affected {#pathways}

DEPDC5 participates in **1 Reactome pathway** (⚕ = disease pathway):

| Pathway (Reactome) | Evidence |
| --- | --- |
| [Amino acids regulate mTORC1](https://reactome.org/content/detail/R-HSA-9639288) | curated |

### Molecular function & processes (GO — experimentally supported) {#go}

**Molecular function:** small GTPase binding, protein-containing complex binding.

**Biological process:** cellular response to amino acid starvation, negative regulation of TORC1 signaling.

## Clinical significance {#significance}

**Likely benign** — review status Multiple submitters *(criteria provided, multiple submitters, no conflicts)*, last evaluated 2026-01-23.

**Submitter consensus:** unanimous (5/5 Likely benign).

**Submission history:** 5 submissions (2016–2026); classifications have been stable.

### Submitter classifications {#submitters}

| Submitter | Classification | Review | Method | Date |
| --- | --- | --- | --- | --- |
| Labcorp Genetics (formerly Invitae), Labcorp | Likely benign | criteria provided, single submitter | clinical testing | 2026-01-23 |
| CeGaT Center for Human Genetics Tuebingen | Likely benign | criteria provided, single submitter | clinical testing | 2025-02-01 |
| Blueprint Genetics | Likely benign | criteria provided, single submitter | clinical testing | 2024-09-07 |
| GeneDx | Likely benign | criteria provided, single submitter | clinical testing | 2020-06-23 |
| Ambry Genetics | Likely benign | criteria provided, single submitter | clinical testing | 2016-08-09 |

## Associated conditions {#conditions}

[familial focal epilepsy with variable foci](https://sugi.bio/atlas/disease/familial-focal-epilepsy-with-variable-foci/).

**Reported phenotype names (ClinVar):** Familial focal epilepsy with variable foci, not provided, Inborn genetic diseases, not specified, AllHighlyPenetrant, none provided.

## Similar variants {#similar}

Related DEPDC5 variant pages (same residue, condition, or type): [DEPDC5 c.1218-1G>A](/variant/depdc5-c-1218-minus-1g-a), [DEPDC5 c.1287+1G>A](/variant/depdc5-c-1287-plus-1g-a), [DEPDC5 c.1324+1G>A](/variant/depdc5-c-1324-plus-1g-a), [DEPDC5 c.1324+1G>T](/variant/depdc5-c-1324-plus-1g-t), [DEPDC5 c.193+1G>T](/variant/depdc5-c-193-plus-1g-t), [DEPDC5 c.2105-1G>A](/variant/depdc5-c-2105-minus-1g-a), [DEPDC5 c.2634-2A>G](/variant/depdc5-c-2634-minus-2a-g), [DEPDC5 c.280-1G>A](/variant/depdc5-c-280-minus-1g-a).

### Data sources & attribution {#sources}

ClinVar (NCBI — public domain, built 2026-10-11); gnomAD v4.1 (Broad Institute, built 2026-10-06); AlphaMissense (Cheng et al. 2023, © Google DeepMind — CC BY 4.0, built 2026-01-27); REVEL (Ioannidis et al. 2016 — ODbL, built 2026-07-13); SaProt (Su et al. 2023 — MIT, built 2026-07-14); SpliceAI (Illumina — free for non-commercial use, built 2026-10-13); CADD (Rentzsch et al. 2019, University of Washington — free for non-commercial use, built 2026-10-10); Conservation (phyloP/phastCons/GERP) (UCSC hg38 470-way mammal (Hiller Lab) + Ensembl Compara, built 2026-07-12); gnomAD Non-coding Constraint (Gnocchi) (Chen et al. 2024, Broad Institute — CC0, built 2026-10-11); gnomAD Regional Missense Constraint (Broad Institute — CC0, built 2026-10-13); Pangolin (Zeng & Li 2022 — CC BY 4.0, built 2026-10-11); Repeat regions (UCSC — RepeatMasker, TRF, segmental duplications, built 2026-10-11); ClinGen (ClinGen, built 2026-09-22); UniProt (CC BY 4.0); Reactome / GO (CC BY 4.0, built 2026-09-23); MaveDB (per-record license, built 2026-10-11); CIViC (CC0, built 2026-09-22); Orphanet (Orphanet, built 2026-06-12)

*Primary record: NCBI ClinVar (variation 444584). Classifications reflect these databases as of the page's build date and may change. Free reference use — not medical advice; consult the primary submitters and a clinician.*