Duplication | NM_000051.4(ATM):c.5971dup (p.Glu1991fs) | ATM | Pathogenic | 11 | 108183189 | 108183190 | T | TG | criteria provided, single submitter | - |
Deletion | NM_000051.4(ATM):c.6049_6052del (p.Ser2017fs) | ATM | Pathogenic | 11 | 108186591 | 108186594 | ATAGT | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000051.4(ATM):c.6108T>G (p.Tyr2036Ter) | ATM | Pathogenic | 11 | 108186750 | 108186750 | T | G | criteria provided, single submitter | - |
Duplication | NM_000051.4(ATM):c.6177dup (p.Arg2060fs) | ATM | Pathogenic | 11 | 108186818 | 108186819 | C | CA | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000051.4(ATM):c.6415G>T (p.Glu2139Ter) | ATM | Pathogenic | 11 | 108190748 | 108190748 | G | T | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_000051.4(ATM):c.6523dup (p.Arg2175fs) | ATM | Pathogenic | 11 | 108192097 | 108192098 | C | CA | criteria provided, single submitter | - |
Insertion | NM_000051.4(ATM):c.7159_7160insAGCC (p.Phe2387Ter) | ATM | Pathogenic | 11 | 108199817 | 108199818 | T | TAGCC | criteria provided, single submitter | - |
single nucleotide variant | NM_000051.4(ATM):c.7194C>A (p.Tyr2398Ter) | ATM | Pathogenic | 11 | 108199852 | 108199852 | C | A | criteria provided, single submitter | - |
Insertion | NM_000051.4(ATM):c.7261_7262insT (p.Lys2421fs) | ATM | Pathogenic | 11 | 108199919 | 108199920 | A | AT | criteria provided, single submitter | - |
Indel | NM_000051.4(ATM):c.7267_7270delinsTAC (p.Glu2423fs) | ATM | Pathogenic | 11 | 108199925 | 108199928 | GAAG | TAC | criteria provided, single submitter | - |