| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.91107421A>G | CA241230519 | LUM | c.862+697T>C (n.862+697T>C) n.612+697T>C n.255+697T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.91107421A= | CA2054318792 | LUM | c.862+697T= (n.862+697T=) n.612+697T= n.255+697T= | dbSNP |