| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.100731231G>A | CA971456 | VCAM1 | c.1238G>A (p.Gly413Asp) c.*787G>A (n.*787G>A) c.962G>A (p.Gly321Asp) c.929-1187G>A (n.929-1187G>A) c.1052G>A (p.Gly351Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.100731231G>C | CA971455 | VCAM1 | c.1238G>C (p.Gly413Ala) c.*787G>C (n.*787G>C) c.962G>C (p.Gly321Ala) c.929-1187G>C (n.929-1187G>C) c.1052G>C (p.Gly351Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |