Is AFF1 p.Pro884Leu (c.2651C>T) pathogenic?

AFF1 p.Pro884Leu (c.2651C>T) is classified Likely benign in AFF1 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-06-01). AlphaMissense: likely benign (0.1039); Rare (popmax 0.893%, amr).

How common is AFF1 p.Pro884Leu (c.2651C>T) in the general population?

AFF1 p.Pro884Leu (c.2651C>T) is rare (popmax 0.893%, amr) (gnomAD).

What do computational predictors say about AFF1 p.Pro884Leu (c.2651C>T)?

AlphaMissense predicts likely benign (score 0.1039) — an in-silico prediction, not a clinical call.

AFF1 p.Pro884Leu

c.2651C>T · VCV3904797

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.1039 · ACMG-weighted

gnomAD v4.1

Rare

rare (popmax 0.893%, amr)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.1039	likely benign
REVEL	0.212	benign-leaning
SaProt	LLR -7.80	tolerated
⇒ AlphaMissense, REVEL and SaProt all call this tolerated.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 4	GERP 2.1, phastCons 1
Regional constraint	o/e 1.07	unconstrained · MANE · 84 kb · p 0.031 · regional, not allelic
Overall
CADD	23.0	PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

⚠ Isoform check: AlphaMissense numbered on a different transcript (AM P877L vs ClinVar P884L) — verify the residue.

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.893% Admixed American · 536/60,024 alleles

Filtering AF 0.83% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.806%

Overall 0.414% 6,684/1,614,168 alleles · rare

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.893%	112
Remaining individualsnot grpmax-eligible	0.466%	215
European (non-Finnish)	0.453%	221
Middle Eastern	0.429%	233
Ashkenazi Jewishnot grpmax-eligible	0.405%	247
Finnishnot grpmax-eligible	0.244%	410
South Asian	0.166%	603
Amishnot grpmax-eligible	0.11%	912
African / African-American	0.072%	1,390
East Asian	0.00223%	44,878

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene: AFF1
Protein: p.Pro884Leu
Coding: c.2651C>T
MANE Select: NM_001166693
Type: single nucleotide variant
Location: chr4:87126176 (GRCh38)
Gene constraint: LOEUF 0.49 · pLI 0.95 (gnomAD)
Structure: AlphaFold pLDDT 53.06 · 1 PDB
Residue 884: the 'disordered' region

Full AFF1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

AFF1 c.1191+8C>T Benign/Likely benign ★★ same type
AFF1 p.Ala40= Benign ★★ same type
AFF1 p.Pro393= Benign ★★ same type
AFF1 p.Ser627Cys Likely benign ★★ same type
AFF1 p.Thr426= Likely benign ★★ same type
AFF1 p.Val711Ile Benign ★★ same type
AFF1 p.Ala1047Val Uncertain significance ★ ⚠ same type
AFF1 p.Ala1103Thr Uncertain significance ★ ⚠ same type

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/aff1-p-pro884leu (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown