Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Indel | NM_000051.4(ATM):c.4343_4344delinsGTT (p.Leu1448fs) | ATM | Pathogenic | 11 | 108160435 | 108160436 | TA | GTT | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000051.4(ATM):c.4579del (p.Val1528fs) | ATM | Pathogenic | 11 | 108163485 | 108163485 | AC | A | criteria provided, single submitter | - |
single nucleotide variant | NM_000051.4(ATM):c.4957C>T (p.Gln1653Ter) | ATM | Pathogenic | 11 | 108168061 | 108168061 | C | T | criteria provided, single submitter | - |
Deletion | NM_000051.4(ATM):c.6280del (p.Glu2094fs) | ATM | Pathogenic | 11 | 108188181 | 108188181 | TG | T | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_000051.4(ATM):c.6555dup (p.Gly2186fs) | ATM | Pathogenic | 11 | 108192128 | 108192129 | A | AT | criteria provided, single submitter | - |
Deletion | NM_000051.4(ATM):c.6843del (p.Gln2280_Tyr2281insTer) | ATM | Pathogenic | 11 | 108196820 | 108196820 | AC | A | criteria provided, single submitter | - |
Deletion | NM_000051.4(ATM):c.7608del (p.His2538fs) | ATM | Pathogenic | 11 | 108202263 | 108202263 | GA | G | criteria provided, single submitter | - |
Insertion | NM_000051.4(ATM):c.7655_7656insGA (p.His2552fs) | ATM | Pathogenic | 11 | 108202630 | 108202631 | C | CAG | criteria provided, single submitter | - |
Duplication | NM_000051.4(ATM):c.8249dup (p.Leu2750fs) | ATM | Pathogenic | 11 | 108206667 | 108206668 | A | AT | criteria provided, single submitter | - |
Deletion | NC_000011.10:g.(?_108243943)_(108365518_?)del | ATM | Pathogenic | 11 | 108114670 | 108236245 | na | na | criteria provided, single submitter | - |