Send feedback

EMP2 p.Thr98=

c.294C>A · rs2142171096 · VCV3029451

Likely benign No assertion criteria
Classification
Likely benign
ClinVar
Review
No assertion criteria ☆☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1
Conditions
1
EMP2-related disorder

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI—not assessed · no allele here is in the release
Constraint at this position
ConservationphyloP -0.3GERP -2.5, phastCons 0.011
Overall
CADD4.063PHRED · no single calibrated threshold — expert panels disagree

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
EMP2
Protein
p.Thr98=
Coding
c.294C>A
MANE Select
NM_001424
dbSNP
rs2142171096
Type
single nucleotide variant
Location
chr16:10537950 (GRCh38)
Gene constraint
LOEUF 1.855 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 94.89
Full EMP2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

EMP2-related disorder

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/emp2-p-thr98 (accessed [today's date]).

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