| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.88998060G>A | CA13446397 | GRM5 | c.661+49152C>T (n.661+49152C>T) c.725+10975C>T (n.725+10975C>T) c.223+10975C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.88998060G>T | CA1989826966 | GRM5 | c.661+49152C>A (n.661+49152C>A) c.725+10975C>A (n.725+10975C>A) c.223+10975C>A | dbSNP |