Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.68422693A>C | CA715188425 | ITGA11 | c.52+9322T>G (n.52+9322T>G) | dbSNP |
15 | g.68422693A>G | CA15858653 | ITGA11 | c.52+9322T>C (n.52+9322T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.68422693A= | CA2184975719 | ITGA11 | c.52+9322T= (n.52+9322T=) | dbSNP |