Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.22731420T>A | CA4185468 | IL6 | c.486T>A (p.Asp162Glu) c.417T>A (p.Asp139Glu) c.258T>A (p.Asp86Glu) n.711T>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.22731420T>C | CA453974200 | IL6 | c.486T>C (p.Asp162=) c.417T>C (p.Asp139=) c.258T>C (p.Asp86=) n.711T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |