Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.46834716C>T | CA698553671 | HTR2A | c.*121G>A (n.*121G>A) | dbSNP gnomAD v4 |
13 | g.46834716C>G | CA13830706 | HTR2A | c.*121G>C (n.*121G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.46834716C= | CA2018007826 | HTR2A | c.*121G= (n.*121G=) | dbSNP |