single nucleotide variant | NM_024675.4(PALB2):c.3441T>A (p.Cys1147Ter) | PALB2 | Pathogenic | 16 | 23614900 | 23614900 | A | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_024675.4(PALB2):c.3425T>A (p.Leu1142Ter) | PALB2 | Pathogenic | 16 | 23614916 | 23614916 | A | T | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_024675.4(PALB2):c.2619del (p.Ser873fs) | PALB2 | Likely pathogenic | 16 | 23637686 | 23637686 | CA | C | criteria provided, single submitter | - |
Deletion | NM_024675.4(PALB2):c.2100_2110del (p.Ser701fs) | PALB2 | Pathogenic | 16 | 23641365 | 23641375 | AGTAATATGGAT | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_024675.4(PALB2):c.1845del (p.Asp616fs) | PALB2 | Likely pathogenic | 16 | 23641630 | 23641630 | CA | C | criteria provided, single submitter | - |
Deletion | NM_024675.4(PALB2):c.1789del (p.Met597fs) | PALB2 | Pathogenic | 16 | 23641686 | 23641686 | AT | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_024675.4(PALB2):c.1288C>T (p.Gln430Ter) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23646579 | 23646579 | G | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_024675.4(PALB2):c.1227_1231del (p.Tyr409_Arg411delinsTer) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23646636 | 23646640 | CTAACA | C | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_024675.4(PALB2):c.841del (p.Ile281fs) | PALB2 | Likely pathogenic | 16 | 23647026 | 23647026 | AT | A | criteria provided, single submitter | - |
Duplication | NM_024675.4(PALB2):c.820dup (p.Thr274fs) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23647046 | 23647047 | G | GT | criteria provided, multiple submitters, no conflicts | - |