Deletion | NM_000051.4(ATM):c.964_968del (p.Glu322fs) | ATM | Pathogenic | 11 | 108117751 | 108117755 | AATGAG | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656195 |
Duplication | NM_000051.4(ATM):c.441dup (p.Asp148fs) | ATM | Pathogenic | 11 | 108106503 | 108106504 | C | CA | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656155 |
Duplication | NM_000051.4(ATM):c.442dup (p.Asp148fs) | ATM | Pathogenic | 11 | 108106506 | 108106507 | A | AG | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656156 |
single nucleotide variant | NM_000051.4(ATM):c.1003G>T (p.Gly335Ter) | ATM | Pathogenic/Likely pathogenic | 11 | 108117792 | 108117792 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA382531372 |
single nucleotide variant | NM_000051.4(ATM):c.1178G>A (p.Trp393Ter) | ATM | Pathogenic | 11 | 108119772 | 108119772 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA382532540 |
Deletion | NM_000051.4(ATM):c.1464del (p.Trp488fs) | ATM | Pathogenic | 11 | 108121655 | 108121655 | TG | T | criteria provided, single submitter | ClinGen:CA658656146 |
single nucleotide variant | NM_000051.4(ATM):c.73-1G>A | ATM | Pathogenic/Likely pathogenic | 11 | 108098502 | 108098502 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA382519448 |
Duplication | NM_000051.4(ATM):c.2749dup (p.Ser917fs) | ATM | Pathogenic | 11 | 108139246 | 108139247 | G | GT | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656142 |
single nucleotide variant | NM_000051.4(ATM):c.2838+1G>T | ATM | Likely pathogenic | 11 | 108139337 | 108139337 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA382545873 |
single nucleotide variant | NM_000051.4(ATM):c.186-1G>A | ATM | Likely pathogenic | 11 | 108099904 | 108099904 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA382520987 |