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CRX p.Asp271fs

c.812del · VCV3759416

Conflicting classifications of pathogenicity Conflicting submitters
Classification
Conflicting classifications of pathogenicity
ClinVar
Review
Conflicting submitters ★☆☆☆
ClinVar · 2 submitters
Consequence
frameshift
predicted LoF
gnomAD v4.1
Rare
Conditions
3
CRX-related disorders

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Consequenceframeshiftpredicted loss-of-function
NMDescapespremature termination codon in the last exon (4 of 4) — the truncated protein is likely expressed. PVS1 input, not an applied code
Splicing
SpliceAI—not assessed · substitutions only
Constraint at this position
ConservationphyloP 11GERP 0.68, phastCons 1

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

Variant & gene context

Gene
CRX
Protein
p.Asp271fs
Coding
c.812del
MANE Select
NM_000554
Type
Deletion
Location
chr19:47839879 (GRCh38)
Gene constraint
LOEUF 0.673 · pLI 0.72 · ClinGen HI 1/3 (gnomAD)
Structure
AlphaFold pLDDT 61.78 · 1 PDB
Full CRX gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

CRX-related disorders

Also linked: cone-rod dystrophy 2Leber congenital amaurosis 7

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/crx-p-asp271fs (accessed [today's date]).

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