Is SON p.Arg1979His (c.5936G>A) pathogenic?

SON p.Arg1979His (c.5936G>A) is classified Uncertain significance in SON (ClinVar, Single submitter, 1 submitter; last evaluated 2023-02-09). AlphaMissense: likely pathogenic (0.89); Very rare (popmax 0.00391%, amr).

How common is SON p.Arg1979His (c.5936G>A) in the general population?

SON p.Arg1979His (c.5936G>A) is very rare (popmax 0.00391%, amr) (gnomAD).

What do computational predictors say about SON p.Arg1979His (c.5936G>A)?

AlphaMissense predicts likely pathogenic (score 0.89) — an in-silico prediction, not a clinical call.

SON p.Arg1979His

c.5936G>A · rs977567856 · VCV2974565

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.89 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.00391%, amr)

Missense predictors

2/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.89	likely pathogenic
REVEL	0.214	benign-leaning
SaProt	LLR -11.49	damaging
⇒ AlphaMissense and SaProt call this damaging; REVEL does not.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Regional constraint	o/e 0.62	unconstrained · MANE · 2,181 bp · p 1.3e-08 · regional, not allelic
Overall
CADD	24.3	PHRED · no single calibrated threshold — expert panels disagree

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

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00391% Admixed American · 2/51,204 alleles

Filtering AF 0.000648% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.000321%

Overall 0.000782% 12/1,534,726 alleles · very rare exomes 11/1,384,940 · genomes 1/149,786 · joint denominator

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.00391%	25,602
European (non-Finnish)	0.000871%	114,821

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: SON
Protein: p.Arg1979His
Coding: c.5936G>A
MANE Select: NM_138927
dbSNP: rs977567856
Type: single nucleotide variant
Location: chr21:33555167 (GRCh38)
Gene constraint: LOEUF 0.051 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 36.48 · 4 PDB
Residue 1979: the 'disordered' region; the '7 x 7 aa repeats of p-s-r-r-s-r-[ts]' region; the '2 x 19 aa repeats of p-s-r-r-r-r-s-r-s-v-v-r-r-r-s-f-s-i-s' region

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

Similar variants

SON p.Arg1979Ser Uncertain significance ★ ⚠ same residue
SON p.Arg1979Cys Likely benign ★ ⚠ same residue
SON c.6321+1G>A Pathogenic ★★ same type
SON p.Arg1081Ter Pathogenic ★★ same type
SON p.Arg1112Ter Pathogenic ★★ same type
SON p.Arg1825Ter Pathogenic ★★ same type
SON p.Arg2008Ter Pathogenic ★★ same type
SON p.Gln96Ter Pathogenic/Likely pathogenic ★★ 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/son-p-arg1979his (accessed [today's date]).

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