The NM_177438.3:c.2951A>G variant in DICER1 is a missense variant predicted to cause substitution of asparagine by serine at amino acid 984 (p.Asn984Ser). Although this variant has been observed in germline cases, to our knowledge, this variant has not been reported in individuals with DICER1-related tumor predisposition (PS4 not met; Internal lab contributors). This variant has been seen in 40 or more unrelated females without tumors through age 50 in at least one testing laboratory (BS2; Internal lab contributors). The total allele frequency in gnomAD v4.1.0 is 0.00002603 (42/1613822 alleles) with a highest population minor allele frequency of 0.0001068 (8/74908 alleles) in the African/African American population (PM2_Supporting, BS1, and BA1 are not met). Two different missense variants, c.2950A>C (p.Asn984His) and c.2952C>A (p.Asn984Lys), in the same codon have been reported (ClinVar Variation ID: 2716149, 1015034). However, these variants have not yet met the criteria to be classified as pathogenic by the ClinGen DICER VCEP (PM5 not met). In silico tools predict no damaging impact of the variant on protein function (REVEL: 0.136; MaxEntScan and SpliceAI: no effect on splicing) (BP4). In summary, this variant meets the criteria to be classified as likely benign for DICER1-related tumor predisposition based on the ACMG/AMP criteria applied, as specified by the ClinGen DICER1 VCEP: BS2, BP4. (Bayesian Points: -5; VCEP specifications version 1.3.0; 01/07/2025).