Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.113932382G>T | CA6284055 | HTR3B | c.462G>T (p.Ala154=) c.429G>T (p.Ala143=) c.248G>T c.261G>T (p.Ala87=) c.255G>T (p.Ala85=) c.168G>T (p.Ala56=) n.713G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.113932382G>C | CA6284054 | HTR3B | c.462G>C (p.Ala154=) c.429G>C (p.Ala143=) c.248G>C c.261G>C (p.Ala87=) c.255G>C (p.Ala85=) c.168G>C (p.Ala56=) n.713G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.113932382G>A | CA6284053 | HTR3B | c.462G>A (p.Ala154=) c.429G>A (p.Ala143=) c.248G>A c.261G>A (p.Ala87=) c.255G>A (p.Ala85=) c.168G>A (p.Ala56=) n.713G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |