Deletion | NM_024675.4(PALB2):c.2818del (p.Glu940fs) | PALB2 | Pathogenic | 16 | 23635346 | 23635346 | TC | T | criteria provided, single submitter | ClinGen:CA658658402 |
Deletion | NM_024675.4(PALB2):c.1704_1707del (p.Lys569fs) | PALB2 | Pathogenic | 16 | 23641768 | 23641771 | CTTTT | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658658418 |
Deletion | NM_024675.4(PALB2):c.1565del (p.Pro522fs) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23646302 | 23646302 | TG | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA645583278 |
Deletion | NM_024675.4(PALB2):c.1490del (p.Asn497fs) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23646377 | 23646377 | AT | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA658658421 |
Duplication | NM_024675.4(PALB2):c.442_457dup (p.Arg153fs) | PALB2 | Pathogenic | 16 | 23647409 | 23647410 | C | CTCTTCTGCTGCTTCTT | criteria provided, multiple submitters, no conflicts | ClinGen:CA658658445 |
Deletion | NM_024675.4(PALB2):c.2915del (p.Leu972fs) | PALB2 | Pathogenic | 16 | 23634371 | 23634371 | CA | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658658397 |
single nucleotide variant | NM_024675.4(PALB2):c.1702C>T (p.Gln568Ter) | PALB2 | Pathogenic | 16 | 23641773 | 23641773 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA395128442 |
Duplication | NM_024675.4(PALB2):c.801_802dup (p.Lys268fs) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23647064 | 23647065 | T | TTA | criteria provided, multiple submitters, no conflicts | ClinGen:CA658658440 |
Deletion | NM_024675.4(PALB2):c.514_517del (p.Ser172fs) | PALB2 | Pathogenic | 16 | 23647350 | 23647353 | CCAGA | C | reviewed by expert panel | ClinGen:CA658658444 |
single nucleotide variant | NM_024675.4(PALB2):c.3165C>G (p.Tyr1055Ter) | PALB2 | Pathogenic | 16 | 23625361 | 23625361 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA395141266 |