# NM_000169.3(GLA):c.797A>T (p.Asp266Val)

https://sugi.bio/variant/gla-p-asp266val

## Summary

**GLA p.Asp266Val (c.797A>T)** is classified **Pathogenic** in GLA (ClinVar, Multiple submitters, 6 submitters; last evaluated 2026-09-08). AlphaMissense: likely pathogenic (0.9727); Very rare (popmax 0.00175%, afr); Associated with Fabry disease.

**At a glance:** Pathogenic · review: Multiple submitters · rsID rs28935487 · 6 submitters · 1 linked condition · AlphaMissense likely pathogenic · very rare (popmax 0.00175%, afr)

## For patients & families {#patients}

This is a change in the GLA gene that is considered disease-causing, submitted by 6 submitters, and is linked to Fabry disease.

*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) | X-linked dominant, X-linked recessive |
| Age of onset (of this condition) | Adolescent, Adult, Childhood |
| Prevalence | 1-9 / 1 000 000 (Worldwide) |
| Clinical trials | 228 registered for this condition — see ClinicalTrials.gov |
| Diagnostic panels | GLA is a diagnostic-grade gene on 27 Genomics England panels |

**Commonly reported features of Fabry disease** (across patients with this condition; presentation varies — frequencies from Orphanet):

- Renal insufficiency — Very frequent (99-80%)
- Nephrotic syndrome — Very frequent (99-80%)
- Hearing impairment — Very frequent (99-80%)
- Conjunctival telangiectasia — Very frequent (99-80%)
- Hematuria — Very frequent (99-80%)
- Hyperkeratosis — Very frequent (99-80%)
- Hypohidrosis — Very frequent (99-80%)
- Angiokeratoma — Very frequent (99-80%)

**Support & next steps:** [Condition overview & support (NIH GARD)](https://rarediseases.info.nih.gov/diseases/0006400/index) · [Find a genetic counselor (NSGC)](https://findageneticcounselor.nsgc.org/).

## Identity {#identity}

| Field | Value |
| --- | --- |
| Gene | [GLA](https://sugi.bio/atlas/gene/GLA/) |
| Protein change (HGVS p.) | p.Asp266Val |
| Coding change (HGVS c.) | c.797A>T |
| MANE Select transcript | [NM_000169](https://www.ncbi.nlm.nih.gov/nuccore/NM_000169) |
| dbSNP | [rs28935487](https://www.ncbi.nlm.nih.gov/snp/rs28935487/) |
| Variant type | single nucleotide variant |
| Location | chrX:101398789-101398789 (GRCh38) |
| ClinVar | [VCV10735](https://www.ncbi.nlm.nih.gov/clinvar/variation/10735/) |

**All HGVS expressions:** `LRG_672:g.14175A>T`, `LRG_672t1:c.797A>T`, `NC_000023.10:g.100653777T>A`, `NC_000023.11:g.101398789T>A`, `NG_007119.1:g.14175A>T`, `NM_000169.3:c.797A>T`, `NM_001199973.2:c.300+3332T>A`, `NM_001199974.2:c.177+6967T>A`, `NM_001406747.1:c.920A>T`, `NM_001406748.1:c.797A>T`, `NR_164783.1:n.876A>T`, `NR_176252.1:n.727A>T`, `NR_176253.1:n.934A>T`

## Computational & population evidence {#evidence}

**Concordance:** 1 independent predictor **concordant** with the ClinVar classification.

- AlphaMissense **likely pathogenic** (0.9727) — concordant with the pathogenic call
- REVEL 0.974 (strongly pathogenic-leaning) — agrees with AlphaMissense
- SaProt LLR -14.54 (damaging) — agrees with AlphaMissense
- → **In-silico consensus:** AlphaMissense, REVEL and SaProt all call this damaging
- Conservation: phyloP 7.856, GERP 3.44, phastCons 1 — highly conserved (agrees)
- AlphaMissense ranks this among the **top 2%** most-pathogenic-predicted substitutions in GLA (of 2,527 modeled).
- CADD: **PHRED 28.3**. 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.*
- Regional missense constraint: **o/e 0.66** across the covering region of the MANE Select transcript (101,397,812–101,403,879), spanning 6,067 bp. Chi-square p 6.6e-08. Describes the region, not this allele; gnomAD v4.1.1's own constrained determination. *Descriptive; no ACMG code applied.*
- SpliceAI: **below the reporting threshold**. This position is scored for a different substitution (T>C, Δ0.97 donor 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 **0.00175%** (afr) · 1/57,168 in the highest group · 1/111,873 alleles overall — very rare (popmax 0.00175%, afr).

*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}

**GLA** population constraint: 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):

- **Fabry disease** — Definitive (XL)

## Protein context {#protein}

Residue **266** lies in a UniProt-annotated variant site (in fabryd).

AlphaFold model confidence (whole protein): pLDDT 94.45, 90% of residues very-high.

**31 experimental structure(s)** (PDB): [1R46](https://www.rcsb.org/structure/1R46), [1R47](https://www.rcsb.org/structure/1R47), [3GXN](https://www.rcsb.org/structure/3GXN), [3GXP](https://www.rcsb.org/structure/3GXP), [3GXT](https://www.rcsb.org/structure/3GXT), [3HG2](https://www.rcsb.org/structure/3HG2).

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

*Describes the biological roles of GLA (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:** GLA's established molecular role includes catalytic activity.


### Pathways affected {#pathways}

GLA participates in **2 Reactome pathways** (⚕ = disease pathway):

| Pathway (Reactome) | Evidence |
| --- | --- |
| [Glycosphingolipid catabolism](https://reactome.org/content/detail/R-HSA-9840310) | curated |
| [Neutrophil degranulation](https://reactome.org/content/detail/R-HSA-6798695) | curated |

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

**Molecular function:** catalytic activity, alpha-galactosidase activity, signaling receptor binding, protein homodimerization activity.

**Biological process:** oligosaccharide metabolic process, glycosphingolipid catabolic process.

## Clinical significance {#significance}

**Pathogenic** — review status Multiple submitters *(criteria provided, multiple submitters, no conflicts)*, last evaluated 2026-09-08.

**Submitter consensus:** unanimous (6/6 Pathogenic).

**Submission history:** 6 submissions (1993–2026); classifications have been stable.

### Submitter classifications {#submitters}

| Submitter | Classification | Review | Method | Date |
| --- | --- | --- | --- | --- |
| Women's Health and Genetics/Laboratory Corporation of America, LabCorp | Pathogenic | criteria provided, single submitter | clinical testing | 2021-01-12 |
| OMIM | Pathogenic | no assertion criteria provided | literature only | 1993-12-01 |
| Eurofins Ntd Llc (ga) | Pathogenic | criteria provided, single submitter | clinical testing | 2018-05-23 |
| Labcorp Genetics (formerly Invitae), Labcorp | Pathogenic | criteria provided, single submitter | clinical testing | 2025-02-16 |
| Genome-Nilou Lab | Pathogenic | criteria provided, single submitter | clinical testing | 2021-07-15 |
| Genomenon, Inc, Genomenon, Inc | Pathogenic | criteria provided, single submitter | curation | 2026-09-08 |

## Associated conditions {#conditions}

[Fabry disease](https://sugi.bio/atlas/disease/fabry-disease/).

**Reported phenotype names (ClinVar):** Fabry disease, not provided, none provided, Ceramide trihexosidosis, Fabry's disease, CERAMIDE TRIHEXOSIDASE DEFICIENCY, GLA DEFICIENCY, HEREDITARY DYSTOPIC LIPIDOSIS, ALPHA-GALACTOSIDASE A DEFICIENCY, ANDERSON-FABRY DISEASE.

## Same-residue context {#hotspot}

Residue **266** carries **4 other pathogenic ClinVar variants** — a recurrently-mutated position: [GLA p.Asp266Asn](/variant/gla-p-asp266asn), [GLA p.Asp266Glu](/variant/gla-p-asp266glu), [GLA p.Asp266Gly](/variant/gla-p-asp266gly), [GLA p.Asp266Tyr](/variant/gla-p-asp266tyr). *Positional co-occurrence of independent ClinVar records, not functional proof.*

## Similar variants {#similar}

Related GLA variant pages (same residue, condition, or type): [GLA p.Asp266Asn](/variant/gla-p-asp266asn), [GLA p.Asp266Glu](/variant/gla-p-asp266glu), [GLA p.Asp266Gly](/variant/gla-p-asp266gly), [GLA p.Asp266Tyr](/variant/gla-p-asp266tyr), [GLA p.Asp266Ala](/variant/gla-p-asp266ala), [GLA p.Asp266His](/variant/gla-p-asp266his), [GLA p.Asp266=](/variant/gla-p-asp266), [GLA c.1000-10G>A](/variant/gla-c-1000-minus-10g-a).

### Data sources & attribution {#sources}

ClinVar (NCBI — public domain, built 2026-10-14); 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 10735). 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.*