Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_001613.4(ACTA2):c.138G>T (p.Met46Ile) | ACTA2 | Pathogenic/Likely pathogenic | 10 | 90707135 | 90707135 | C | A | criteria provided, multiple submitters, no conflicts | - |