Deletion | NM_000051.4(ATM):c.689del (p.Asn230fs) | ATM | Pathogenic/Likely pathogenic | 11 | 108115539 | 108115539 | TA | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16043454 |
single nucleotide variant | NM_000051.4(ATM):c.497-1G>A | ATM | Likely pathogenic | 11 | 108114679 | 108114679 | G | A | criteria provided, single submitter | ClinVar:424841,ClinGen:CA6264624 |
single nucleotide variant | NM_000051.4(ATM):c.1236-2A>T | ATM | Pathogenic | 11 | 108121426 | 108121426 | A | T | criteria provided, multiple submitters, no conflicts | ClinVar:424841,ClinGen:CA6264792 |
single nucleotide variant | NM_000051.4(ATM):c.4106C>A (p.Ser1369Ter) | ATM | Pathogenic/Likely pathogenic | 11 | 108158439 | 108158439 | C | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA16606070 |
single nucleotide variant | NM_000051.4(ATM):c.6096-2A>G | ATM | Pathogenic/Likely pathogenic | 11 | 108186736 | 108186736 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA501172 |
single nucleotide variant | NM_000051.4(ATM):c.2115C>G (p.Tyr705Ter) | ATM | Pathogenic/Likely pathogenic | 11 | 108124757 | 108124757 | C | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA16606161 |
single nucleotide variant | NM_000051.4(ATM):c.901+1G>C | ATM | Pathogenic | 11 | 108115754 | 108115754 | G | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA16606776 |
single nucleotide variant | NM_000051.4(ATM):c.8641C>T (p.Gln2881Ter) | ATM | Pathogenic | 11 | 108218062 | 108218062 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16606855 |
Deletion | NC_000011.10:g.(?_108222832)_(108369099_?)del | ATM | Pathogenic | 11 | 108093559 | 108239826 | na | na | criteria provided, single submitter | - |
Deletion | NM_000051.4(ATM):c.1212_1213del (p.Gln404_Asn405insTer) | ATM | Pathogenic | 11 | 108119805 | 108119806 | CAG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA16612981 |