single nucleotide variant | NM_000478.6(ALPL):c.809G>A (p.Trp270Ter) | ALPL | Pathogenic/Likely pathogenic | 1 | 21896814 | 21896814 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA274277 |
single nucleotide variant | NM_000478.6(ALPL):c.791A>G (p.Lys264Arg) | ALPL | Pathogenic/Likely pathogenic | 1 | 21894739 | 21894739 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA273908 |
single nucleotide variant | NM_000478.6(ALPL):c.667C>T (p.Arg223Trp) | ALPL | Pathogenic/Likely pathogenic | 1 | 21894615 | 21894615 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA274235,UniProtKB:P05186#VAR_013986 |
single nucleotide variant | NM_000478.6(ALPL):c.542C>T (p.Ser181Leu) | ALPL | Pathogenic/Likely pathogenic | 1 | 21890603 | 21890603 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA273974,UniProtKB:P05186#VAR_013982 |
Indel | NM_000478.6(ALPL):c.400_401delinsCA (p.Thr134His) | ALPL | Pathogenic/Likely pathogenic | 1 | 21889705 | 21889706 | AC | CA | criteria provided, multiple submitters, no conflicts | ClinGen:CA274069 |
single nucleotide variant | NM_000478.6(ALPL):c.215T>C (p.Ile72Thr) | ALPL | Pathogenic/Likely pathogenic | 1 | 21887623 | 21887623 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA274142 |
single nucleotide variant | NM_000478.6(ALPL):c.814C>T (p.Arg272Cys) | ALPL | Pathogenic | 1 | 21896819 | 21896819 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA256936,OMIM:171760.0023 |
single nucleotide variant | NM_000478.6(ALPL):c.526G>A (p.Ala176Thr) | ALPL | Pathogenic/Likely pathogenic | 1 | 21890587 | 21890587 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA256935,UniProtKB:P05186#VAR_011083,OMIM:171760.0022 |
single nucleotide variant | NM_000478.6(ALPL):c.1366G>A (p.Gly456Arg) | ALPL | Pathogenic | 1 | 21903932 | 21903932 | G | A | criteria provided, single submitter | ClinGen:CA256934,UniProtKB:P05186#VAR_011091,OMIM:171760.0019 |
single nucleotide variant | NM_000478.6(ALPL):c.1250A>G (p.Asn417Ser) | ALPL | Pathogenic/Likely pathogenic | 1 | 21903075 | 21903075 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA199266,UniProtKB:P05186#VAR_025937,OMIM:171760.0017 |