single nucleotide variant | NM_024675.4(PALB2):c.2630G>A (p.Trp877Ter) | PALB2 | Pathogenic | 16 | 23637675 | 23637675 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10579959 |
Indel | NM_024675.4(PALB2):c.2482_2504delinsAAGGTACAAT (p.Cys828fs) | PALB2 | Pathogenic | 16 | 23640971 | 23640993 | GAATGTTTATGCAGCTCCTGGCA | ATTGTACCTT | criteria provided, single submitter | ClinGen:CA10579965 |
Deletion | NM_024675.4(PALB2):c.2488del (p.Glu830fs) | PALB2 | Pathogenic | 16 | 23640987 | 23640987 | TC | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10579966 |
Deletion | NM_024675.4(PALB2):c.2470del (p.Cys824fs) | PALB2 | Pathogenic | 16 | 23641005 | 23641005 | CA | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA10579969 |
Duplication | NM_024675.4(PALB2):c.2325dup (p.Phe776fs) | PALB2 | Pathogenic | 16 | 23641149 | 23641150 | A | AT | criteria provided, multiple submitters, no conflicts | ClinGen:CA10579974 |
Deletion | NM_024675.4(PALB2):c.2296_2297del (p.Val767fs) | PALB2 | Pathogenic | 16 | 23641178 | 23641179 | TGA | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10579975 |
Deletion | NM_024675.4(PALB2):c.2288_2291del (p.His762_Leu763insTer) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23641184 | 23641187 | TTTCA | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA10579976 |
Deletion | NM_024675.4(PALB2):c.2280del (p.Ala761fs) | PALB2 | Pathogenic | 16 | 23641195 | 23641195 | CA | C | criteria provided, single submitter | ClinGen:CA10579977 |
Deletion | NM_024675.4(PALB2):c.2156del (p.Pro719fs) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23641319 | 23641319 | AG | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA10579983 |
Insertion | NM_024675.4(PALB2):c.2142_2143insTAA (p.Asp715Ter) | PALB2 | Pathogenic | 16 | 23641332 | 23641333 | C | CTTA | criteria provided, single submitter | ClinGen:CA10579984 |