Deletion | NM_024675.4(PALB2):c.2092del (p.Leu698fs) | PALB2 | Pathogenic | 16 | 23641383 | 23641383 | AG | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16609596 |
Deletion | NM_024675.4(PALB2):c.1817_1818del (p.Phe606fs) | PALB2 | Pathogenic | 16 | 23641657 | 23641658 | GAA | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA16609597 |
Deletion | NM_024675.4(PALB2):c.1591_1592del (p.Leu531fs) | PALB2 | Pathogenic | 16 | 23646275 | 23646276 | CAA | C | criteria provided, single submitter | ClinGen:CA16609598 |
Duplication | NM_024675.4(PALB2):c.1186dup (p.Cys396fs) | PALB2 | Pathogenic | 16 | 23646680 | 23646681 | C | CA | criteria provided, multiple submitters, no conflicts | ClinGen:CA16609599 |
Duplication | NM_024675.4(PALB2):c.1114dup (p.Ser372fs) | PALB2 | Pathogenic | 16 | 23646752 | 23646753 | C | CT | criteria provided, multiple submitters, no conflicts | ClinGen:CA16609600 |
Deletion | NM_024675.4(PALB2):c.1047_1050del (p.Asn349fs) | PALB2 | Pathogenic | 16 | 23646817 | 23646820 | TTTGA | T | criteria provided, single submitter | ClinGen:CA16609601 |
single nucleotide variant | NM_024675.4(PALB2):c.1039G>T (p.Glu347Ter) | PALB2 | Pathogenic | 16 | 23646828 | 23646828 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16609602 |
Duplication | NM_024675.4(PALB2):c.976dup (p.Ser326fs) | PALB2 | Pathogenic | 16 | 23646890 | 23646891 | G | GA | criteria provided, multiple submitters, no conflicts | ClinGen:CA16609603 |
single nucleotide variant | NM_024675.4(PALB2):c.931A>T (p.Lys311Ter) | PALB2 | Pathogenic | 16 | 23646936 | 23646936 | T | A | criteria provided, single submitter | ClinGen:CA16609604 |
Deletion | NM_024675.4(PALB2):c.759del (p.Ser254fs) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23647108 | 23647108 | AT | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16609605 |