Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.71151778T>A | CA239490105 | TSPAN8 | c.60+5841A>T (n.60+5841A>T) n.319+5122A>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.71151778T= | CA2045155765 | TSPAN8 | c.60+5841A= (n.60+5841A=) n.319+5122A= | dbSNP |