Classification rationale
1
The BRCA2 c.9014_9015del (p.Arg3005IlefsTer12) variant has not been observed in COSMIC and has been reported in ClinVar as pathogenic, including ENIGMA expert panel review.
clinvar ↗2
This variant is absent from gnomAD v2.1 and gnomAD v4.1, although ENIGMA does not apply PM2_Supporting to insertion, deletion, or delins variants.
gnomad_v2 ↗ gnomad_v4 ↗ cspec ↗3
ENIGMA BRCA2 null-variant guidance supports full-strength PVS1 for truncating variants in exon 23 and assigns PM5_PTC Strong to this exon, consistent with a deleterious premature termination event.
cspec ↗4
SpliceAI predicts possible splice impact with a maximum delta score of 0.23.
spliceai ↗