single nucleotide variant | NM_024675.4(PALB2):c.2066C>A (p.Ser689Ter) | PALB2 | Pathogenic | 16 | 23641409 | 23641409 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584512 |
Deletion | NM_024675.4(PALB2):c.1714del (p.Ser572fs) | PALB2 | Likely pathogenic | 16 | 23641761 | 23641761 | GA | G | criteria provided, single submitter | ClinGen:CA10584515 |
Deletion | NM_024675.4(PALB2):c.1538del (p.Thr513fs) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23646329 | 23646329 | TG | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584518 |
single nucleotide variant | NM_024675.4(PALB2):c.472C>T (p.Gln158Ter) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23647395 | 23647395 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584523 |
Duplication | NM_024675.4(PALB2):c.12dup (p.Pro5fs) | PALB2 | Pathogenic | 16 | 23652466 | 23652467 | G | GA | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584526 |
single nucleotide variant | NM_024675.4(PALB2):c.1A>G (p.Met1Val) | PALB2 | Likely pathogenic | 16 | 23652478 | 23652478 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA10584527 |
Deletion | NM_024675.4(PALB2):c.3295_3301del (p.Thr1099fs) | PALB2 | Likely pathogenic | 16 | 23619234 | 23619240 | AGAGTCGT | A | criteria provided, single submitter | ClinGen:CA10588599 |
single nucleotide variant | NM_024675.4(PALB2):c.3234T>A (p.Cys1078Ter) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23619301 | 23619301 | A | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10588601 |
single nucleotide variant | NM_024675.4(PALB2):c.3114-1G>A | PALB2 | Likely pathogenic | 16 | 23625413 | 23625413 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10588602 |
Deletion | NM_024675.4(PALB2):c.3041_3042del (p.Leu1014fs) | PALB2 | Likely pathogenic | 16 | 23632754 | 23632755 | TTA | T | criteria provided, single submitter | ClinGen:CA10588603 |