Is ANKS6 p.Pro57Ser (c.169C>T) pathogenic?

ANKS6 p.Pro57Ser (c.169C>T) is classified Uncertain significance in ANKS6 (ClinVar, Single submitter, 1 submitter; last evaluated 2025-05-19). AlphaMissense: likely benign (0.0831); Very rare (popmax 0.000305%, nfe); Associated with Inborn genetic diseases.

What condition is associated with ANKS6 p.Pro57Ser (c.169C>T)?

ANKS6 p.Pro57Ser (c.169C>T) is associated with Inborn genetic diseases (ClinVar).

How common is ANKS6 p.Pro57Ser (c.169C>T) in the general population?

ANKS6 p.Pro57Ser (c.169C>T) is very rare (popmax 0.000305%, nfe) (gnomAD).

What do computational predictors say about ANKS6 p.Pro57Ser (c.169C>T)?

AlphaMissense predicts likely benign (score 0.0831) — an in-silico prediction, not a clinical call.

ANKS6 p.Pro57Ser

c.169C>T · VCV3918617

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.0831 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.000305%, nfe)

Missense predictors

0/3 damaging

AlphaMissense, REVEL, SaProt

Conditions

Inborn genetic diseases

Computational evidence

Protein change
AlphaMissense	0.0831	likely benign
REVEL	0.07	moderately benign-leaning
SaProt	LLR -6.60	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 2.2	GERP -1.3, phastCons 1
Regional constraint	o/e 0.99	unconstrained · MANE · 60 kb · p 0.79 · regional, not allelic
Overall
CADD	15.05	PHRED · no single calibrated threshold — expert panels disagree

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

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

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.000305% European (non-Finnish) · 3/982,106 alleles

Filtering AF 8.1e-05% ClinGen BA1/BS1 input FAF95, joint · FAF99 2.3e-05%

Overall 0.00028% 3/1,070,848 alleles · very rare

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: ANKS6
Protein: p.Pro57Ser
Coding: c.169C>T
MANE Select: NM_173551
Type: single nucleotide variant
Location: chr9:98796323 (GRCh38)
Gene constraint: LOEUF 0.869 · pLI <0.01 · ClinGen HI gene assoc. with recessive phenotype (gnomAD)
Structure: AlphaFold pLDDT 60.60 · 1 PDB

Full ANKS6 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

ANKS6 p.Ala363Val Uncertain significance ★★ ⚠ same condition
ANKS6 p.Ala589Glu Uncertain significance ★★ ⚠ same condition
ANKS6 p.Ala64Pro Uncertain significance ★★ ⚠ same condition
ANKS6 p.Ala835Thr Uncertain significance ★★ ⚠ same condition
ANKS6 p.Ala9Val Uncertain significance ★★ ⚠ same condition
ANKS6 p.Arg142Gln Uncertain significance ★★ ⚠ same condition
ANKS6 p.Arg153Trp Uncertain significance ★★ ⚠ same condition
ANKS6 p.Arg427Trp Uncertain significance ★★ ⚠ same condition

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/anks6-p-pro57ser (accessed [today's date]).

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