# NM_022437.3(ABCG8):c.1333T>G (p.Phe445Val)

https://sugi.bio/variant/abcg8-p-phe445val

## Summary

**ABCG8 p.Phe445Val (c.1333T>G)** is classified **Uncertain significance** in ABCG8 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2023-08-04). AlphaMissense: likely benign (0.1023); Ultra-rare (popmax 0.0495%, mid); Associated with sitosterolemia 1.

**At a glance:** Uncertain significance · review: Multiple submitters · rsID rs376492876 · 2 submitters · 1 linked condition · AlphaMissense likely benign · ultra-rare (popmax 0.0495%, mid)

## For patients & families {#patients}

This is a change in the ABCG8 gene that is currently of uncertain significance — a definitive interpretation has not yet been established, submitted by 2 submitters, and is linked to sitosterolemia 1.

*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) | All ages |
| Diagnostic panels | ABCG8 is a diagnostic-grade gene on 11 Genomics England panels |

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

- Xanthomatosis — Frequent (79-30%)
- Splenomegaly — Frequent (79-30%)
- Hemolytic anemia — Frequent (79-30%)
- Giant platelets — Frequent (79-30%)
- Arthralgia — Frequent (79-30%)
- Elevated circulating hepatic transaminase concentration — Frequent (79-30%)
- Hypercholesterolemia — Frequent (79-30%)
- Stomatocytosis — Frequent (79-30%)

**Support & next steps:** [Condition overview & support (NIH GARD)](https://rarediseases.info.nih.gov/diseases/0025235/index) · [Find a genetic counselor (NSGC)](https://findageneticcounselor.nsgc.org/).

## Identity {#identity}

| Field | Value |
| --- | --- |
| Gene | [ABCG8](https://sugi.bio/atlas/gene/ABCG8/) |
| Protein change (HGVS p.) | p.Phe445Val |
| Coding change (HGVS c.) | c.1333T>G |
| MANE Select transcript | [NM_022437](https://www.ncbi.nlm.nih.gov/nuccore/NM_022437) |
| dbSNP | [rs376492876](https://www.ncbi.nlm.nih.gov/snp/rs376492876/) |
| Variant type | single nucleotide variant |
| Location | chr2:43873908-43873908 (GRCh38) |
| ClinVar | [VCV1520342](https://www.ncbi.nlm.nih.gov/clinvar/variation/1520342/) |

**All HGVS expressions:** `LRG_1182:g.46967T>G`, `LRG_1182t1:c.1333T>G`, `NC_000002.11:g.44101047T>G`, `NC_000002.12:g.43873908T>G`, `NG_008884.2:g.46967T>G`, `NM_001357321.2:c.1330T>G`, `NM_022437.3:c.1333T>G`

## Computational & population evidence {#evidence}

**Concordance:** ClinVar classifies this **uncertain**; the computational predictors unanimously lean **tolerated** — a triage signal, not a reclassification.

- AlphaMissense **likely benign** (0.1023)
- REVEL 0.083 (moderately benign-leaning) — agrees with AlphaMissense
- SaProt LLR -5.676 (tolerated) — agrees with AlphaMissense
- → **In-silico consensus:** AlphaMissense, REVEL and SaProt all call this tolerated
- Conservation: phyloP -0.593, GERP -3.08 — not a conserved position (phyloP < 0.1, ACGS BP7 cut)
- CADD: **PHRED 0.371**. 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 1.29** across the covering region of the MANE Select transcript (43,839,054–43,877,910), spanning 38,856 bp. Chi-square p 8.8e-18. Describes the region, not this allele; gnomAD v4.1.1's own constrained determination. *Descriptive; no ACMG code 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 **0.0495%** (mid) · FAF95 0.0134% · FAF99 0.00718% · 3/6,062 in the highest group · 5/1,614,188 alleles overall — ultra-rare (popmax 0.0495%, mid).

| Ancestry group | Allele frequency | 1 in |
| --- | --- | --- |
| Middle Eastern (grpmax) | 0.0495% | 2,021 |
| European (non-Finnish) | 0.000169% | 590,019 |

*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}

**ABCG8** population constraint: LOEUF 1.329, pLI 5.1931e-31, missense-Z -2.6097; ClinGen dosage — haploinsufficiency 30, 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):

- **sitosterolemia** — Definitive (AR)

## Protein context {#protein}

Residue **445** lies in the abc transmembrane type-2 domain; an α-helix.

AlphaFold model confidence (whole protein): pLDDT 80.94, 39% of residues very-high.

**8 experimental structure(s)** (PDB): [5DO7](https://www.rcsb.org/structure/5DO7), [7JR7](https://www.rcsb.org/structure/7JR7), [7R87](https://www.rcsb.org/structure/7R87), [7R88](https://www.rcsb.org/structure/7R88), [7R89](https://www.rcsb.org/structure/7R89), [7R8A](https://www.rcsb.org/structure/7R8A).

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

*Describes the biological roles of ABCG8 (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:** ABCG8's established molecular role includes ATPase-coupled transmembrane transporter activity. p.Phe445Val falls in the abc transmembrane type-2 domain. In Reactome, ABCG8 is annotated in disease pathway(s) including **Defective ABCG5 causes sitosterolemia**, **Defective ABCG8 causes GBD4 and sitosterolemia**.

**Disease mechanism (Reactome):** ABCG8 loss or alteration is curated in [Defective ABCG5 causes sitosterolemia](https://reactome.org/content/detail/R-HSA-5679096), [Defective ABCG8 causes GBD4 and sitosterolemia](https://reactome.org/content/detail/R-HSA-5679090).

### Pathways affected {#pathways}

ABCG8 participates in **4 Reactome pathways** (⚕ = disease pathway):

| Pathway (Reactome) | Evidence |
| --- | --- |
| ⚕ [Defective ABCG5 causes sitosterolemia](https://reactome.org/content/detail/R-HSA-5679096) | curated |
| ⚕ [Defective ABCG8 causes GBD4 and sitosterolemia](https://reactome.org/content/detail/R-HSA-5679090) | curated |
| [ABC transporters in lipid homeostasis](https://reactome.org/content/detail/R-HSA-1369062) | curated |
| [NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport and efflux](https://reactome.org/content/detail/R-HSA-9029569) | curated |

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

**Molecular function:** ATPase-coupled transmembrane transporter activity, protein heterodimerization activity.

**Biological process:** negative regulation of intestinal phytosterol absorption, cholesterol efflux, cholesterol homeostasis, negative regulation of intestinal cholesterol absorption.

## Clinical significance {#significance}

**Uncertain significance** — review status Multiple submitters *(criteria provided, multiple submitters, no conflicts)*, last evaluated 2023-08-04.

**Submitter consensus:** unanimous (2/2 Uncertain significance).

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

### Submitter classifications {#submitters}

| Submitter | Classification | Review | Method | Date |
| --- | --- | --- | --- | --- |
| Revvity Omics, Revvity | Uncertain significance | criteria provided, single submitter | clinical testing | 2023-02-28 |
| Labcorp Genetics (formerly Invitae), Labcorp | Uncertain significance | criteria provided, single submitter | clinical testing | 2023-08-04 |

## Associated conditions {#conditions}

[sitosterolemia 1](https://sugi.bio/atlas/disease/sitosterolemia-1/).

**Reported phenotype names (ClinVar):** Sitosterolemia 1, not provided, none provided.

## Similar variants {#similar}

Related ABCG8 variant pages (same residue, condition, or type): [ABCG8 p.Phe445=](/variant/abcg8-p-phe445), [ABCG8 p.Phe445Leu](/variant/abcg8-p-phe445leu), [ABCG8 c.64-2A>G](/variant/abcg8-c-64-minus-2a-g), [ABCG8 c.965-1G>C](/variant/abcg8-c-965-minus-1g-c), [ABCG8 p.Arg164Ter](/variant/abcg8-p-arg164ter), [ABCG8 p.Arg405Cys](/variant/abcg8-p-arg405cys), [ABCG8 p.Arg412Ter](/variant/abcg8-p-arg412ter), [ABCG8 p.Gly574Arg](/variant/abcg8-p-gly574arg).

### 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 1520342). 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.*