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RET p.Pro60fs

c.179_180del · VCV4907067

Likely pathogenic Single submitter
Classification
Likely pathogenic
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
Consequence
frameshift
predicted LoF
gnomAD v4.1
Rare
Conditions
1
RET-related disorder

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequenceframeshiftpredicted loss-of-function in a haploinsufficient gene (ClinGen)
NMDpredictedpremature termination codon in exon 2 of 20
Splicing
SpliceAI—not assessed · substitutions only
Constraint at this position
ConservationphyloP 1.8GERP 1.7, phastCons 0.36

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

Variant & gene context

Gene
RET
Protein
p.Pro60fs
Coding
c.179_180del
MANE Select
NM_020975
Type
Deletion
Location
chr10:43100564 (GRCh38)
Gene constraint
LOEUF 0.24 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure
AlphaFold pLDDT 79.27 · 34 PDB
Residue 60
the 'cadherin-like region 1 (cld1)' region
Full RET gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

RET-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/ret-p-pro60fs (accessed [today's date]).

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