Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.68157416G>C | CA2043752255 | IFNG | c.366+497C>G (n.366+497C>G) | dbSNP |
12 | g.68157416G>T | CA948825461 | IFNG | c.366+497C>A (n.366+497C>A) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.68157416G>A | CA238116526 | IFNG | c.366+497C>T (n.366+497C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |