Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.161629864G>T | CA1212467 | FCGR3B | c.230C>A (p.Ala77Asp) n.609C>A c.40+1191C>A (n.40+1191C>A) c.61+504C>A (n.61+504C>A) n.150C>A c.233C>A (p.Ala78Asp) c.294C>A c.341C>A (p.Ala114Asp) n.387C>A c.182C>A (p.Ala61Asp) c.338C>A (p.Ala113Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.161629864G>A | CA343352092 | FCGR3B | c.230C>T (p.Ala77Val) n.609C>T c.40+1191C>T (n.40+1191C>T) c.61+504C>T (n.61+504C>T) n.150C>T c.233C>T (p.Ala78Val) c.294C>T c.341C>T (p.Ala114Val) n.387C>T c.182C>T (p.Ala61Val) c.338C>T (p.Ala113Val) | dbSNP gnomAD v4 |