Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.88824823A>C | CA1989740032 | GRM5 | c.911+25083T>G (n.911+25083T>G) | dbSNP |
11 | g.88824823A>G | CA15677919 | GRM5 | c.911+25083T>C (n.911+25083T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.88824823A>T | CA1989740031 | GRM5 | c.911+25083T>A (n.911+25083T>A) | dbSNP |