Duplication | NM_003998.4(NFKB1):c.830dup (p.Lys278fs) | NFKB1 | Pathogenic/Likely pathogenic | 4 | 103501790 | 103501791 | C | CA | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_012452.3(TNFRSF13B):c.492C>G (p.Tyr164Ter) | TNFRSF13B | Pathogenic/Likely pathogenic | 17 | 16843779 | 16843779 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA203874 |
Deletion | NM_012452.3(TNFRSF13B):c.49del (p.Gln17fs) | TNFRSF13B | Pathogenic/Likely pathogenic | 17 | 16875341 | 16875341 | TG | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA658798719 |
single nucleotide variant | NM_012452.3(TNFRSF13B):c.311G>A (p.Cys104Tyr) | TNFRSF13B | Pathogenic/Likely pathogenic | 17 | 16852186 | 16852186 | C | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000377.3(WAS):c.809T>C (p.Leu270Pro) | WAS | Pathogenic/Likely pathogenic | X | 48546720 | 48546720 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA280988,UniProtKB:P42768#VAR_033256,OMIM:300392.0012 |
single nucleotide variant | NM_000377.3(WAS):c.881T>C (p.Ile294Thr) | WAS | Pathogenic/Likely pathogenic | X | 48546792 | 48546792 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA281104,OMIM:300392.0025 |
single nucleotide variant | NM_000377.3(WAS):c.91G>A (p.Glu31Lys) | WAS | Pathogenic/Likely pathogenic | X | 48542333 | 48542333 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA412865672 |