Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
Deletion | NC_000012.12:g.(?_132660959)_(132661174_?)del | POLE | Pathogenic | 12 | 133237545 | 133237760 | na | na | criteria provided, single submitter | - |
single nucleotide variant | NM_006231.4(POLE):c.1021-1G>C | POLE | Likely pathogenic | 12 | 133252407 | 133252407 | C | G | criteria provided, single submitter | - |
single nucleotide variant | NM_006231.4(POLE):c.4445-2A>C | POLE | Likely pathogenic | 12 | 133219918 | 133219918 | T | G | criteria provided, single submitter | - |
single nucleotide variant | NM_006231.4(POLE):c.4006-2A>T | POLE | Likely pathogenic | 12 | 133225660 | 133225660 | T | A | criteria provided, single submitter | - |
Deletion | NM_006231.4(POLE):c.1226+2_1226+5del | POLE | Likely pathogenic | 12 | 133251979 | 133251982 | CCCTA | C | criteria provided, single submitter | - |