CINP — 2 ClinVar variants
All ClinVar germline CINP variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 1 flagged for review →
1 Likely pathogenic · 1 Benign
Full CINP gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 1
Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.
Predictors split 1
The independent predictors disagree with each other — read with care.
All CINP variants
Likely pathogenic 1
- p.Ter213Gly Single submitter intellectual disability
Benign 1
- p.Arg164His Multiple submitters ⚠