Is MAP2K1 p.Ser364Phe (c.1091C>T) pathogenic?

MAP2K1 p.Ser364Phe (c.1091C>T) is classified Uncertain significance in MAP2K1 (ClinVar, Single submitter, 1 submitter; last evaluated 2022-07-27). AlphaMissense: ambiguous (0.4462); Absent from gnomAD v4.1.

How common is MAP2K1 p.Ser364Phe (c.1091C>T) in the general population?

MAP2K1 p.Ser364Phe (c.1091C>T) is absent from gnomAD v4.1 (gnomAD).

What do computational predictors say about MAP2K1 p.Ser364Phe (c.1091C>T)?

AlphaMissense predicts ambiguous (score 0.4462) — an in-silico prediction, not a clinical call.

MAP2K1 p.Ser364Phe

c.1091C>T · rs1893220220 · VCV2413054

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

ambiguous

0.4462 · ACMG-weighted

gnomAD v4.1

Absent

absent from gnomAD v4.1

Computational evidence

Protein change
AlphaMissense	0.4462	ambiguous
REVEL	0.52	indeterminate
SaProt	LLR -4.92	tolerated
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP 7.7	GERP 2.1, phastCons 1
Regional constraint	o/e 0.61	unconstrained · MANE · 5,593 bp · p 6.7e-08 · regional, not allelic
Overall
CADD	25.4	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

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene: MAP2K1
Protein: p.Ser364Phe
Coding: c.1091C>T
MANE Select: NM_002755
dbSNP: rs1893220220
Type: single nucleotide variant
Location: chr15:66490524 (GRCh38)
Gene constraint: LOEUF 0.515 · pLI 0.97 · ClinGen HI 0/3 (gnomAD)
Structure: AlphaFold pLDDT 84.05 · 99 PDB
Residue 364: an α-helix

Full MAP2K1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

MAP2K1 p.Ser364Tyr Uncertain significance ★ same residue
MAP2K1 p.Ser364= Likely benign ★ same residue
MAP2K1 p.Arg108Leu Likely pathogenic ★★★ same type
MAP2K1 p.Asn122Asp Pathogenic ★★★ ⚠ same type
MAP2K1 p.Asp67Asn Pathogenic ★★★ same type
MAP2K1 p.Glu203Gly Pathogenic ★★★ same type
MAP2K1 p.Leu42Arg Likely pathogenic ★★★ same type
MAP2K1 p.Leu42Phe 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/map2k1-p-ser364phe (accessed [today's date]).

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