single nucleotide variant | NM_000053.4(ATP7B):c.813C>A (p.Cys271Ter) | ATP7B | Pathogenic | 13 | 52548543 | 52548543 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA274145 |
single nucleotide variant | NM_000053.4(ATP7B):c.841C>T (p.Gln281Ter) | ATP7B | Likely pathogenic | 13 | 52548515 | 52548515 | G | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000053.4(ATP7B):c.845del (p.Leu282fs) | ATP7B | Pathogenic | 13 | 52548511 | 52548511 | GA | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA260157 |
single nucleotide variant | NM_000053.4(ATP7B):c.865C>T (p.Gln289Ter) | ATP7B | Pathogenic/Likely pathogenic | 13 | 52548491 | 52548491 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA252900,OMIM:606882.0022 |
single nucleotide variant | NM_000053.4(ATP7B):c.915T>A (p.Cys305Ter) | ATP7B | Pathogenic | 13 | 52548441 | 52548441 | A | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA220313 |
single nucleotide variant | NM_000053.4(ATP7B):c.970A>T (p.Lys324Ter) | ATP7B | Pathogenic/Likely pathogenic | 13 | 52548386 | 52548386 | T | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000053.4(ATP7B):c.994G>T (p.Glu332Ter) | ATP7B | Pathogenic | 13 | 52548362 | 52548362 | C | A | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000053.4(ATP7B):c.1063C>T (p.Gln355Ter) | ATP7B | Pathogenic/Likely pathogenic | 13 | 52548293 | 52548293 | G | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000053.4(ATP7B):c.1145_1151del (p.Ser382fs) | ATP7B | Pathogenic/Likely pathogenic | 13 | 52548205 | 52548211 | CAGTTGGG | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA484024617 |
Deletion | NM_000053.4(ATP7B):c.1158_1159del (p.Val387fs) | ATP7B | Pathogenic | 13 | 52548197 | 52548198 | ACC | A | criteria provided, multiple submitters, no conflicts | - |