# NM_182760.4(SUMF1):c.825C>T (p.Phe275=)

https://sugi.bio/variant/sumf1-p-phe275

## Summary

**SUMF1 p.Phe275= (c.825C>T)** is classified **Likely benign** in SUMF1 (ClinVar, Single submitter, 2 submitters; last evaluated 2023-09-21). Very rare (popmax 0.00333%, amr); Associated with mucosulfatidosis.

**At a glance:** Likely benign · review: Single submitter · rsID rs780668525 · 2 submitters · 1 linked condition · very rare (popmax 0.00333%, amr)

## For patients & families {#patients}

This is a change in the SUMF1 gene that is classified as likely benign — not considered disease-causing, submitted by 2 submitters, and is linked to mucosulfatidosis.

*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 recessive |
| Age of onset (of this condition) | Adolescent, Antenatal, Childhood, Infancy, Neonatal |
| Clinical trials | 6 registered for this condition — see ClinicalTrials.gov |
| Diagnostic panels | SUMF1 is a diagnostic-grade gene on 15 Genomics England panels |

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

- Visual impairment — Very frequent (99-80%)
- Intellectual disability — Very frequent (99-80%)
- Global developmental delay — Very frequent (99-80%)
- Neonatal hypotonia — Very frequent (99-80%)
- Splenomegaly — Very frequent (99-80%)
- Hepatomegaly — Very frequent (99-80%)
- Developmental regression — Very frequent (99-80%)
- Abnormality of peripheral nerve conduction — Very frequent (99-80%)

**Support & next steps:** [Condition overview & support (NIH GARD)](https://rarediseases.info.nih.gov/diseases/0005061/index) · [Find a genetic counselor (NSGC)](https://findageneticcounselor.nsgc.org/).

## Identity {#identity}

| Field | Value |
| --- | --- |
| Gene | [SUMF1](https://sugi.bio/atlas/gene/SUMF1/) |
| Protein change (HGVS p.) | p.Phe275= |
| Coding change (HGVS c.) | c.825C>T |
| MANE Select transcript | [NM_182760](https://www.ncbi.nlm.nih.gov/nuccore/NM_182760) |
| dbSNP | [rs780668525](https://www.ncbi.nlm.nih.gov/snp/rs780668525/) |
| Variant type | single nucleotide variant |
| Location | chr3:4417143-4417143 (GRCh38) |
| ClinVar | [VCV793527](https://www.ncbi.nlm.nih.gov/clinvar/variation/793527/) |

**All HGVS expressions:** `NC_000003.11:g.4458827G>A`, `NC_000003.12:g.4417143G>A`, `NG_016225.2:g.55140C>T`, `NM_001164674.2:c.750C>T`, `NM_001164675.2:c.825C>T`, `NM_182760.4:c.825C>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 6.576, GERP 0.675, phastCons 1 — highly conserved position (PP3-type support)
- CADD: **PHRED 12.98**. 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: **not assessed** — no allele at this position is in our SpliceAI release, either because it lies outside the scored MANE transcript scope or because every allele is below Δ0.2. We cannot tell which, so this claims neither; absence is not evidence against a splicing effect.
- Population frequency (gnomAD v4.1): grpmax **0.00333%** (amr) · FAF95 0.000553% · FAF99 0.000207% · 2/60,010 in the highest group · 5/1,613,872 alleles overall — very rare (popmax 0.00333%, amr).

| Ancestry group | Allele frequency | 1 in |
| --- | --- | --- |
| Admixed American (grpmax) | 0.00333% | 30,005 |
| Remaining individuals (not grpmax-eligible) | 0.0016% | 62,494 |
| South Asian | 0.0011% | 91,070 |
| European (non-Finnish) | 8.48e-05% | 1,179,864 |

*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}

**SUMF1** population constraint: LOEUF 1.254, pLI 1.2003e-16, missense-Z -1.3757. *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):

- **mucosulfatidosis** — Definitive (AR)

## Protein context {#protein}

Residue **275** lies in a binding site.

AlphaFold model confidence (whole protein): pLDDT 85.39, 75% of residues very-high.

**21 experimental structure(s)** (PDB): [1Y1E](https://www.rcsb.org/structure/1Y1E), [1Y1F](https://www.rcsb.org/structure/1Y1F), [1Y1G](https://www.rcsb.org/structure/1Y1G), [1Y1H](https://www.rcsb.org/structure/1Y1H), [1Y1I](https://www.rcsb.org/structure/1Y1I), [1Y1J](https://www.rcsb.org/structure/1Y1J) — incl. mutant structure 2AFT.

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

*Describes the biological roles of SUMF1 (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:** SUMF1's established molecular role includes identical protein binding.


### Pathways affected {#pathways}

SUMF1 participates in **2 Reactome pathways** (⚕ = disease pathway):

| Pathway (Reactome) | Evidence |
| --- | --- |
| [Glycosphingolipid catabolism](https://reactome.org/content/detail/R-HSA-9840310) | curated |
| [The activation of arylsulfatases](https://reactome.org/content/detail/R-HSA-1663150) | curated |

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

**Molecular function:** identical protein binding, formylglycine-generating oxidase activity, cupric ion binding.

**Biological process:** protein oxidation, post-translational protein modification.

## Clinical significance {#significance}

**Likely benign** — review status Single submitter *(criteria provided, single submitter)*, last evaluated 2023-09-21.

**Submitter consensus:** unanimous (2/2 Likely benign).

**Submission history:** 2 submissions (2020–2023); classifications have been stable.

### Submitter classifications {#submitters}

| Submitter | Classification | Review | Method | Date |
| --- | --- | --- | --- | --- |
| Natera, Inc. | Likely benign | no assertion criteria provided | clinical testing | 2020-04-23 |
| Labcorp Genetics (formerly Invitae), Labcorp | Likely benign | criteria provided, single submitter | clinical testing | 2023-09-21 |

## Associated conditions {#conditions}

[mucosulfatidosis](https://sugi.bio/atlas/disease/mucosulfatidosis/).

**Reported phenotype names (ClinVar):** Multiple sulfatase deficiency, Multiple Sulfatase Deficiency Disease, Sulfatidosis, Juvenile, Austin Type, Mucosulfatidosis.

## Similar variants {#similar}

Related SUMF1 variant pages (same residue, condition, or type): [SUMF1 c.271-1G>C](/variant/sumf1-c-271-minus-1g-c), [SUMF1 c.445-1G>A](/variant/sumf1-c-445-minus-1g-a), [SUMF1 c.445-2A>G](/variant/sumf1-c-445-minus-2a-g), [SUMF1 c.520-1G>C](/variant/sumf1-c-520-minus-1g-c), [SUMF1 c.602+1G>A](/variant/sumf1-c-602-plus-1g-a), [SUMF1 c.603-1G>C](/variant/sumf1-c-603-minus-1g-c), [SUMF1 c.840+1G>A](/variant/sumf1-c-840-plus-1g-a), [SUMF1 c.954+1G>T](/variant/sumf1-c-954-plus-1g-t).

### Data sources & attribution {#sources}

ClinVar (NCBI — public domain, built 2026-10-14); gnomAD v4.1 (Broad Institute, built 2026-10-14); 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 2026-10-14); 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 793527). 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.*