single nucleotide variant | NM_024675.4(PALB2):c.2512C>T (p.Gln838Ter) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23640963 | 23640963 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA395123923 |
Duplication | NM_024675.4(PALB2):c.2255_2267dup (p.Cys756fs) | PALB2 | Pathogenic | 16 | 23641207 | 23641208 | G | GCAGCAAGTTCGTC | criteria provided, multiple submitters, no conflicts | ClinGen:CA658658405 |
Deletion | NM_024675.4(PALB2):c.2219_2220del (p.Gln740fs) | PALB2 | Pathogenic | 16 | 23641255 | 23641256 | CTT | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA658658406 |
Insertion | NM_024675.4(PALB2):c.2160_2161insG (p.Thr721fs) | PALB2 | Pathogenic | 16 | 23641314 | 23641315 | T | TC | criteria provided, single submitter | ClinGen:CA658658409 |
Deletion | NM_024675.4(PALB2):c.2002del (p.Met668fs) | PALB2 | Pathogenic | 16 | 23641473 | 23641473 | AT | A | criteria provided, single submitter | ClinGen:CA658658410 |
Deletion | NM_024675.4(PALB2):c.1653del (p.Gln552fs) | PALB2 | Pathogenic | 16 | 23646214 | 23646214 | GA | G | criteria provided, single submitter | ClinGen:CA658658420 |
single nucleotide variant | NM_024675.4(PALB2):c.1648A>T (p.Lys550Ter) | PALB2 | Pathogenic | 16 | 23646219 | 23646219 | T | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA395130127 |
Deletion | NM_024675.4(PALB2):c.905del (p.Asn302fs) | PALB2 | Pathogenic | 16 | 23646962 | 23646962 | GT | G | criteria provided, single submitter | ClinGen:CA658658437 |
Deletion | NM_024675.4(PALB2):c.810_828del (p.Ser270fs) | PALB2 | Pathogenic | 16 | 23647039 | 23647057 | CGTGAGTAGTAAGTTCACTG | C | criteria provided, single submitter | ClinGen:CA658658439 |
single nucleotide variant | NM_024675.4(PALB2):c.814G>T (p.Glu272Ter) | PALB2 | Pathogenic | 16 | 23647053 | 23647053 | C | A | criteria provided, single submitter | ClinGen:CA395135986 |