Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.184060222G>T | CA355379499 | HTR3C | c.1214G>T (p.Gly405Val) | dbSNP |
3 | g.184060222G>A | CA355379498 | HTR3C | c.1214G>A (p.Gly405Glu) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.184060222G>C | CA2725772 | HTR3C | c.1214G>C (p.Gly405Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.184060222G= | CA1425847024 | HTR3C | c.1214G= (p.Gly405=) | dbSNP |