Insertion | NM_000059.4(BRCA2):c.5343_5344insA (p.Gln1782fs) | BRCA2 | Likely pathogenic | 13 | 32913835 | 32913836 | T | TA | criteria provided, single submitter | ClinGen:CA022051 |
single nucleotide variant | NM_000059.4(BRCA2):c.91T>C (p.Trp31Arg) | BRCA2 | Likely pathogenic | 13 | 32893237 | 32893237 | T | C | criteria provided, single submitter | ClinGen:CA026029 |
single nucleotide variant | NM_000059.4(BRCA2):c.8363G>C (p.Trp2788Ser) | BRCA2 | Likely pathogenic | 13 | 32944570 | 32944570 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA025604 |
single nucleotide variant | NM_000059.4(BRCA2):c.8331+1G>T | BRCA2 | Likely pathogenic | 13 | 32937671 | 32937671 | G | T | criteria provided, single submitter | Breast Cancer Information Core (BIC) (BRCA2):8559+1&base_change=G to T,ClinGen:CA025579 |
single nucleotide variant | NM_000059.4(BRCA2):c.8171G>T (p.Gly2724Val) | BRCA2 | Likely pathogenic | 13 | 32937510 | 32937510 | G | T | criteria provided, single submitter | ClinGen:CA025486 |
single nucleotide variant | NM_000059.4(BRCA2):c.7826G>A (p.Gly2609Asp) | BRCA2 | Likely pathogenic | 13 | 32936680 | 32936680 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA025300 |
single nucleotide variant | NM_000059.4(BRCA2):c.7007+5G>C | BRCA2 | Likely pathogenic | 13 | 32921038 | 32921038 | G | C | criteria provided, single submitter | Breast Cancer Information Core (BIC) (BRCA2):7235+5&base_change=G to C,ClinGen:CA024710 |
single nucleotide variant | NM_000059.4(BRCA2):c.631+2T>C | BRCA2 | Likely pathogenic | 13 | 32900752 | 32900752 | T | C | criteria provided, single submitter | ClinGen:CA023850 |
single nucleotide variant | NM_024426.6(WT1):c.1297T>G (p.Cys433Gly) | WT1 | Likely pathogenic | 11 | 32414269 | 32414269 | A | C | criteria provided, single submitter | ClinGen:CA016265,OMIM:607102.0013 |
single nucleotide variant | NM_024426.6(WT1):c.1406A>G (p.Asp469Gly) | WT1 | Likely pathogenic | 11 | 32413559 | 32413559 | T | C | criteria provided, single submitter | ClinGen:CA016344,OMIM:607102.0005 |