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1 records shown · first 60A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases.
PMID 25534848 | DOI 10.1016/j.molimm.2014.11.010 · Molecular immunology · 2015 · 8 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| variant | c.754G>A | “A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases.” | 0.95 | hgvs_regex_v1 |
| gene | C5 | “A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases.” | 0.98 | hgnc_dict_v1 |
| population | Saudi Arabia | “Approximately 40 individual cases have been diagnosed worldwide. Three different C5 mutations c.55C>T:p.Q19X, c.754G>A:p.A252T and c.4426C>T:p.R1476X were diagnosed in index cases from two families who had both presented with recurrent meningococcal disease. p.Q19X and p.R1476X have already been described in North American Black families and more recently p.Q19X in a Saudi family.” | 0.95 | saudi_context_rules_v1 |
| variant | p.A252T | “A complement C5 gene mutation, c.754G>A:p.A252T, is common in the Western Cape, South Africa and found to be homozygous in seven percent of Black African meningococcal disease cases.” | 0.95 | hgvs_regex_v1 |