single nucleotide variant | NM_000169.3(GLA):c.119C>G (p.Pro40Arg) | GLA | Likely pathogenic | X | 100662773 | 100662773 | G | C | criteria provided, single submitter | ClinGen:CA021455 |
Insertion | NM_000169.3(GLA):c.1019_1020insA (p.Trp340Ter) | GLA | Pathogenic/Likely pathogenic | X | 100653067 | 100653068 | C | CT | criteria provided, multiple submitters, no conflicts | ClinGen:CA021286 |
single nucleotide variant | NM_000169.3(GLA):c.613C>A (p.Pro205Thr) | GLA | Pathogenic/Likely pathogenic | X | 100655680 | 100655680 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA021827,UniProtKB:P06280#VAR_000463 |
single nucleotide variant | NM_000169.3(GLA):c.334C>T (p.Arg112Cys) | GLA | Pathogenic | X | 100658834 | 100658834 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA021639,UniProtKB:P06280#VAR_000447,OMIM:300644.0011,ClinVar:10723 |
single nucleotide variant | NM_000169.3(GLA):c.815A>G (p.Asn272Ser) | GLA | Pathogenic/Likely pathogenic | X | 100653542 | 100653542 | T | C | criteria provided, multiple submitters, no conflicts | ClinGen:CA022099,UniProtKB:P06280#VAR_032292,OMIM:300644.0062 |
single nucleotide variant | NM_000169.3(GLA):c.1228A>G (p.Thr410Ala) | GLA | Pathogenic | X | 100652859 | 100652859 | T | C | criteria provided, single submitter | ClinGen:CA021462,UniProtKB:P06280#VAR_032293,OMIM:300644.0059 |
single nucleotide variant | NM_000169.3(GLA):c.666C>A (p.Tyr222Ter) | GLA | Pathogenic | X | 100653908 | 100653908 | G | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA021952,OMIM:300644.0058 |
single nucleotide variant | NM_000169.3(GLA):c.427G>C (p.Ala143Pro) | GLA | Pathogenic/Likely pathogenic | X | 100656740 | 100656740 | C | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA021721,UniProtKB:P06280#VAR_000453,OMIM:300644.0057 |
single nucleotide variant | NM_000169.3(GLA):c.1095T>A (p.Tyr365Ter) | GLA | Pathogenic | X | 100652992 | 100652992 | A | T | criteria provided, single submitter | ClinGen:CA021385,OMIM:300644.0055 |
single nucleotide variant | NM_000169.3(GLA):c.1192G>T (p.Glu398Ter) | GLA | Pathogenic | X | 100652895 | 100652895 | C | A | criteria provided, single submitter | ClinGen:CA021448,OMIM:300644.0033 |