Duplication | NM_000051.4(ATM):c.5894_5900dup (p.Met1967fs) | ATM | Pathogenic/Likely pathogenic | 11 | 108181017 | 108181018 | A | AAAAGTAT | criteria provided, multiple submitters, no conflicts | ClinGen:CA16619205 |
Deletion | NM_000051.4(ATM):c.6059del (p.Gly2020fs) | ATM | Pathogenic | 11 | 108186601 | 108186601 | TG | T | criteria provided, single submitter | ClinGen:CA16619207 |
single nucleotide variant | NM_000051.4(ATM):c.6238T>G (p.Tyr2080Asp) | ATM | Likely pathogenic | 11 | 108188139 | 108188139 | T | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA16619210 |
Duplication | NM_000051.4(ATM):c.6730dup (p.Arg2244fs) | ATM | Pathogenic/Likely pathogenic | 11 | 108196191 | 108196192 | C | CA | criteria provided, multiple submitters, no conflicts | ClinGen:CA16619219 |
Indel | NM_000051.4(ATM):c.6736_6755delinsCA (p.Cys2246_Thr2252delinsHis) | ATM | Likely pathogenic | 11 | 108196200 | 108196219 | TGTATTAAGGACATTCTCAC | CA | criteria provided, single submitter | ClinGen:CA16619220 |
Deletion | NM_000051.4(ATM):c.6754del (p.Thr2252fs) | ATM | Pathogenic | 11 | 108196218 | 108196218 | CA | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA16619221 |
Deletion | NM_000051.4(ATM):c.6920_6923del (p.Leu2307fs) | ATM | Pathogenic | 11 | 108196896 | 108196899 | TCTTG | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA16619223 |
Duplication | NM_000051.4(ATM):c.7347dup (p.Leu2450fs) | ATM | Likely pathogenic | 11 | 108200978 | 108200979 | G | GA | criteria provided, single submitter | ClinGen:CA16619230 |
Deletion | NM_000051.4(ATM):c.7391_7412del (p.Cys2464fs) | ATM | Likely pathogenic | 11 | 108201021 | 108201042 | TTATGTAAAGCAGTTGAAAATTA | T | criteria provided, single submitter | ClinGen:CA16619232 |
single nucleotide variant | NM_000051.4(ATM):c.7630-2A>G | ATM | Pathogenic/Likely pathogenic | 11 | 108202604 | 108202604 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA16619236 |