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HRAS p.Pro167fs

c.490_499dup · VCV4086451

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; NMD-escape possible for C-terminal truncations
Splicing
SpliceAI—not assessed · substitutions only
Constraint at this position
ConservationphyloP 0.98GERP -0.32, phastCons 0.42

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

Variant & gene context

Gene
HRAS
Protein
p.Pro167fs
Coding
c.490_499dup
MANE Select
NM_005343 · reported on NM_176795
Type
Duplication
Location
chr11:533309 (GRCh38)
Gene constraint
LOEUF 0.893 · pLI 0.02 · ClinGen HI 0/3 (gnomAD)
Structure
AlphaFold pLDDT 92.50 · 256 PDB
Residue 167
the 'hypervariable region' region
Full HRAS 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/hras-p-pro167fs (accessed [today's date]).

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