Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.184036506G>T | CA2725093 | HTR3D | c.329G>T (p.Gly110Val) c.107G>T (p.Gly36Val) c.511+1G>T (n.511+1G>T) c.3+1284G>T (n.3+1284G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.184036506G>C | CA2725092 | HTR3D | c.329G>C (p.Gly110Ala) c.107G>C (p.Gly36Ala) c.511+1G>C (n.511+1G>C) c.3+1284G>C (n.3+1284G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.184036506G>A | CA355365571 | HTR3D | c.329G>A (p.Gly110Asp) c.107G>A (p.Gly36Asp) c.511+1G>A (n.511+1G>A) c.3+1284G>A (n.3+1284G>A) | dbSNP |