Deletion | NM_000051.4(ATM):c.4451del (p.Met1484fs) | ATM | Pathogenic/Likely pathogenic | 11 | 108163360 | 108163360 | AT | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656171 |
single nucleotide variant | NM_000051.4(ATM):c.6586A>T (p.Arg2196Ter) | ATM | Pathogenic/Likely pathogenic | 11 | 108196050 | 108196050 | A | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA382554668 |
single nucleotide variant | NM_000051.4(ATM):c.4776+1G>T | ATM | Pathogenic/Likely pathogenic | 11 | 108164205 | 108164205 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA6265538 |
Duplication | NM_000051.4(ATM):c.4885dup (p.Val1629fs) | ATM | Pathogenic | 11 | 108165760 | 108165761 | T | TG | criteria provided, single submitter | ClinGen:CA658656208 |
single nucleotide variant | NM_000051.4(ATM):c.4909+1G>A | ATM | Pathogenic | 11 | 108165787 | 108165787 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA6265571 |
Deletion | NM_000051.4(ATM):c.7858del (p.Val2620fs) | ATM | Pathogenic/Likely pathogenic | 11 | 108203558 | 108203558 | TG | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA658656302 |
single nucleotide variant | NM_000051.4(ATM):c.5319+2T>C | ATM | Pathogenic/Likely pathogenic | 11 | 108172518 | 108172518 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA382542858 |
single nucleotide variant | NM_000051.4(ATM):c.5326G>T (p.Glu1776Ter) | ATM | Pathogenic/Likely pathogenic | 11 | 108173586 | 108173586 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA382543040 |
single nucleotide variant | NM_000051.4(ATM):c.8011-1G>C | ATM | Likely pathogenic | 11 | 108205695 | 108205695 | G | C | criteria provided, single submitter | ClinGen:CA382561831 |
Duplication | NM_000051.4(ATM):c.5402dup (p.Asn1801fs) | ATM | Pathogenic | 11 | 108173658 | 108173659 | G | GA | criteria provided, single submitter | ClinGen:CA658656254 |