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.445C>T (p.Arg149Cys) | ACTA2 | Pathogenic | 10 | 90701551 | 90701551 | G | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA006936,UniProtKB:P62736#VAR_045918,OMIM:102620.0001 |