Is MAP2 p.Ser1398Asn (c.4193G>A) pathogenic?

MAP2 p.Ser1398Asn (c.4193G>A) is classified Uncertain significance in MAP2 (ClinVar, Single submitter, 1 submitter; last evaluated 2024-12-11). AlphaMissense: likely pathogenic (0.8449); Very rare (popmax 0.0056%, nfe).

How common is MAP2 p.Ser1398Asn (c.4193G>A) in the general population?

MAP2 p.Ser1398Asn (c.4193G>A) is very rare (popmax 0.0056%, nfe) (gnomAD).

What do computational predictors say about MAP2 p.Ser1398Asn (c.4193G>A)?

AlphaMissense predicts likely pathogenic (score 0.8449) — an in-silico prediction, not a clinical call.

MAP2 p.Ser1398Asn

c.4193G>A · VCV3870060

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely pathogenic

0.8449 · ACMG-weighted

gnomAD v4.1

Rare

very rare (popmax 0.0056%, nfe)

Missense predictors

2/3 damaging

AlphaMissense, REVEL, SaProt

Computational evidence

Protein change
AlphaMissense	0.8449	likely pathogenic
REVEL	0.207	benign-leaning
SaProt	LLR -10.99	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
Conservation	phyloP 12	GERP 2.4, phastCons 1
Overall
CADD	27.0	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 0.0056% European (non-Finnish) · 66/1,178,266 alleles

Filtering AF 0.00452% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00412%

Overall 0.00422% 68/1,610,314 alleles · very rare exomes 59/1,458,240 · genomes 9/152,074 · joint denominator

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.0056%	17,853
Admixed American	0.00168%	59,582
Remaining individualsnot grpmax-eligible	0.0016%	62,346

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: MAP2
Protein: p.Ser1398Asn
Coding: c.4193G>A
MANE Select: NM_001375505
Type: single nucleotide variant
Location: chr2:209696554 (GRCh38)
Structure: AlphaFold pLDDT 86.07 · 40 PDB

Full MAP2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

MAP2 p.Ala1074Thr Uncertain significance ★★ ⚠ same type
MAP2 p.Ala752Ser Uncertain significance ★★ ⚠ same type
MAP2 p.Arg1715His Uncertain significance ★★ ⚠ same type
MAP2 p.Val1359Ala Uncertain significance ★★ ⚠ same type
MAP2 p.Ala414Ser Benign/Likely benign ★★ same type
MAP2 p.Asp679= Benign ★★ same type
MAP2 p.Gln1760= Benign/Likely benign ★★ same type
MAP2 p.Glu1129= Benign ★★ 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/map2-p-ser1398asn (accessed [today's date]).

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