# NM_000616.5(CD4):c.1080G>A (p.Val360=)

https://sugi.bio/variant/cd4-p-val360

## Summary

**CD4 p.Val360= (c.1080G>A)** is classified **Likely benign** in CD4 (ClinVar, No assertion criteria, 1 submitter; last evaluated 2019-11-16). Rare (popmax 0.411%, afr); Associated with CD4-related disorder.

**At a glance:** Likely benign · review: No assertion criteria · rsID rs34841304 · 1 submitter · 1 linked condition · rare (popmax 0.411%, afr)

## For patients & families {#patients}

This is a change in the CD4 gene that is classified as likely benign — not considered disease-causing, submitted by 1 submitter, and is linked to CD4-related disorder.

*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.*

**Support & next steps:** [Find a genetic counselor (NSGC)](https://findageneticcounselor.nsgc.org/).

## Identity {#identity}

| Field | Value |
| --- | --- |
| Gene | [CD4](https://sugi.bio/atlas/gene/CD4/) |
| Protein change (HGVS p.) | p.Val360= |
| Coding change (HGVS c.) | c.1080G>A |
| MANE Select transcript | [NM_000616](https://www.ncbi.nlm.nih.gov/nuccore/NM_000616) |
| dbSNP | [rs34841304](https://www.ncbi.nlm.nih.gov/snp/rs34841304/) |
| Variant type | single nucleotide variant |
| Location | chr12:6817254-6817254 (GRCh38) |
| ClinVar | [VCV3048523](https://www.ncbi.nlm.nih.gov/clinvar/variation/3048523/) |

**All HGVS expressions:** `NC_000012.11:g.6926420G>A`, `NC_000012.12:g.6817254G>A`, `NG_027688.1:g.32783G>A`, `NG_027688.2:g.32728G>A`, `NM_000616.5:c.1080G>A`, `NM_001195014.3:c.543G>A`, `NM_001195015.3:c.261G>A`, `NM_001195016.3:c.261G>A`, `NM_001195017.3:c.261G>A`, `NM_001382705.1:c.261G>A`, `NM_001382706.1:c.261G>A`, `NM_001382707.1:c.1080G>A`, `NM_001382714.1:c.915G>A`

## 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 3.042, GERP 0.789, phastCons 0.998 — highly conserved position (PP3-type support)
- CADD: **PHRED 5.538**. 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 **0.411%** (afr) · FAF95 0.373% · FAF99 0.359% · 308/74,884 in the highest group · 391/1,605,604 alleles overall — rare (popmax 0.411%, afr).

| Ancestry group | Allele frequency | 1 in |
| --- | --- | --- |
| African / African-American (grpmax) | 0.411% | 243 |
| Admixed American | 0.089% | 1,124 |
| Remaining individuals (not grpmax-eligible) | 0.0273% | 3,658 |
| European (non-Finnish) | 0.00119% | 83,964 |

*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}

**CD4** population constraint: LOEUF 0.673, pLI 0.0060803, missense-Z 1.6912. *Lower LOEUF and higher pLI indicate a gene that tolerates loss-of-function poorly; ClinGen dosage is the curated haploinsufficiency call.*

## Protein context {#protein}

Residue **360** lies in a disulfide bond; the ig-like c2-type 3 domain.

AlphaFold model confidence (whole protein): pLDDT 85.35, 65% of residues very-high.

**84 experimental structure(s)** (PDB): [1CDH](https://www.rcsb.org/structure/1CDH), [1CDI](https://www.rcsb.org/structure/1CDI), [1CDJ](https://www.rcsb.org/structure/1CDJ), [1CDU](https://www.rcsb.org/structure/1CDU), [1CDY](https://www.rcsb.org/structure/1CDY), [1G9M](https://www.rcsb.org/structure/1G9M) — incl. mutant structure 1CDU.

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

*Describes the biological roles of CD4 (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:** CD4's established molecular role includes virus receptor activity. p.Val360= falls in the ig-like c2-type 3 domain. In Reactome, CD4 is annotated in disease pathway(s) including **Binding and entry of HIV virion**, **Nef Mediated CD4 Down-regulation**.

**Disease mechanism (Reactome):** CD4 loss or alteration is curated in [Binding and entry of HIV virion](https://reactome.org/content/detail/R-HSA-173107), [Nef Mediated CD4 Down-regulation](https://reactome.org/content/detail/R-HSA-167590), [Vpu mediated degradation of CD4](https://reactome.org/content/detail/R-HSA-180534).

### Pathways affected {#pathways}

CD4 participates in **13 Reactome pathways** (⚕ = disease pathway):

| Pathway (Reactome) | Evidence |
| --- | --- |
| ⚕ [Binding and entry of HIV virion](https://reactome.org/content/detail/R-HSA-173107) | curated |
| ⚕ [Nef Mediated CD4 Down-regulation](https://reactome.org/content/detail/R-HSA-167590) | curated |
| ⚕ [Vpu mediated degradation of CD4](https://reactome.org/content/detail/R-HSA-180534) | curated |
| [Alpha-defensins](https://reactome.org/content/detail/R-HSA-1462054) | curated |
| [Cargo recognition for clathrin-mediated endocytosis](https://reactome.org/content/detail/R-HSA-8856825) | curated |
| [Clathrin-mediated endocytosis](https://reactome.org/content/detail/R-HSA-8856828) | curated |
| [Co-inhibition by PD-1](https://reactome.org/content/detail/R-HSA-389948) | curated |
| [Downstream TCR signaling](https://reactome.org/content/detail/R-HSA-202424) | curated |
| [Generation of second messenger molecules](https://reactome.org/content/detail/R-HSA-202433) | curated |
| [Other interleukin signaling](https://reactome.org/content/detail/R-HSA-449836) | curated |
| [Phosphorylation of CD3 and TCR zeta chains](https://reactome.org/content/detail/R-HSA-202427) | curated |
| [Translocation of ZAP-70 to Immunological synapse](https://reactome.org/content/detail/R-HSA-202430) | curated |
| [Affinity selection of immunoglobulins](https://reactome.org/content/detail/R-HSA-9938027) | electronic |

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

**Molecular function:** virus receptor activity, zinc ion binding, lipid binding, coreceptor activity, enzyme binding, protein kinase binding.

**Biological process:** T cell differentiation, macrophage differentiation, maintenance of protein location in cell, interleukin-15-mediated signaling pathway, T cell selection, positive regulation of monocyte differentiation.

## Clinical significance {#significance}

**Likely benign** — review status No assertion criteria *(no assertion criteria provided)*, last evaluated 2019-11-16.

**Submitter consensus:** unanimous (1/1 Likely benign).

### Submitter classifications {#submitters}

| Submitter | Classification | Review | Method | Date |
| --- | --- | --- | --- | --- |
| PreventionGenetics, part of Exact Sciences | Likely benign | no assertion criteria provided | clinical testing | 2019-11-16 |

## Associated conditions {#conditions}

[CD4-related disorder](https://sugi.bio/atlas/disease/cd4-related-disorder/).

**Reported phenotype names (ClinVar):** CD4-related disorder, CD4-related condition.

## Similar variants {#similar}

Related CD4 variant pages (same residue, condition, or type): [CD4 p.Leu344=](/variant/cd4-p-leu344), [CD4 p.Ser352Trp](/variant/cd4-p-ser352trp), [CD4 p.Thr444Ala](/variant/cd4-p-thr444ala), [CD4 c.1346+55T>G](/variant/cd4-c-1346-plus-55t-g), [CD4 c.49+35A>G](/variant/cd4-c-49-plus-35a-g), [CD4 c.*91C>A](/variant/cd4-c-star-91c-a), [CD4 c.*92A>G](/variant/cd4-c-star-92a-g), [CD4 p.Arg265Trp](/variant/cd4-p-arg265trp).

### 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 3048523). 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.*