Classification rationale
1
The PALB2 c.2734T>G (p.Trp912Gly) variant has not been observed in COSMIC and has been reported in ClinVar as Uncertain Significance, including expert-panel review.
clinvar ↗2
This variant is absent from gnomAD v2.1 and gnomAD v4.1, placing its observed population frequency below the PALB2 PM2_Supporting threshold of 0.000333%.
gnomad_v2 ↗ gnomad_v4 ↗ cspec ↗3
SpliceAI predicts no significant splice impact for this variant, with a maximum delta score of 0.03, and although REVEL and BayesDel scores are available, the PALB2 expert-panel specification does not use missense computational predictors for PP3 or BP4.
spliceai ↗ cspec ↗