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MARK2 p.Gln88fs

c.261_262del · VCV4912101

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
Consequence
frameshift
predicted LoF
gnomAD v4.1
Rare

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequenceframeshiftpredicted loss-of-function in a LoF-intolerant gene
NMDpredictedpremature termination codon in exon 3 of 19
Splicing
SpliceAI—not assessed · substitutions only
Constraint at this position
ConservationphyloP 11GERP 1.9, phastCons 1

Predicted loss-of-function is descriptive, not an applied PVS1 code.

Variant & gene context

Gene
MARK2
Protein
p.Gln88fs
Coding
c.261_262del
MANE Select
NM_001039469
Type
Deletion
Location
chr11:63895605 (GRCh38)
Gene constraint
LOEUF 0.287 · pLI 1.00 (gnomAD)
Structure
AlphaFold pLDDT 68.21 · 5 PDB
Residue 88
the protein kinase domain; a UniProt-annotated variant site (in mrd76; likely pathogenic); an α-helix
Full MARK2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

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/mark2-p-gln88fs (accessed [today's date]).

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