Deletion | NM_024675.4(PALB2):c.1437_1438del (p.Lys480fs) | PALB2 | Pathogenic | 16 | 23646429 | 23646430 | TTC | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA658683910 |
Deletion | NM_024675.4(PALB2):c.546del (p.Ser183fs) | PALB2 | Pathogenic | 16 | 23647321 | 23647321 | TG | T | criteria provided, single submitter | ClinGen:CA658683923 |
single nucleotide variant | NM_024675.4(PALB2):c.211+1G>A | PALB2 | Likely pathogenic | 16 | 23649170 | 23649170 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA395139005 |
single nucleotide variant | NM_024675.4(PALB2):c.3166C>T (p.Gln1056Ter) | PALB2 | Pathogenic | 16 | 23625360 | 23625360 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA279530832 |
Deletion | NM_024675.4(PALB2):c.1914del (p.Phe638fs) | PALB2 | Pathogenic | 16 | 23641561 | 23641561 | CA | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658683932 |
Duplication | NM_024675.4(PALB2):c.1276dup (p.Glu426fs) | PALB2 | Pathogenic | 16 | 23646590 | 23646591 | T | TC | criteria provided, single submitter | ClinGen:CA658683912 |
single nucleotide variant | NM_024675.4(PALB2):c.3350+2C>G | PALB2 | Likely pathogenic | 16 | 23619183 | 23619183 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA395139182 |
Deletion | NM_024675.4(PALB2):c.1140_1143del (p.Ser380fs) | PALB2 | Pathogenic | 16 | 23646724 | 23646727 | TAAGA | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA621661731 |
Duplication | NM_024675.4(PALB2):c.1032_1033dup (p.Leu345fs) | PALB2 | Pathogenic | 16 | 23646833 | 23646834 | A | AAG | criteria provided, multiple submitters, no conflicts | ClinGen:CA658683915 |
Deletion | NM_024675.4(PALB2):c.3228del (p.Cys1078fs) | PALB2 | Pathogenic | 16 | 23619307 | 23619307 | GA | G | criteria provided, single submitter | ClinGen:CA658683911 |