Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.40622992A>G | CA7482906 | KNL1 | c.2728A>G (p.Arg910Gly) c.2806A>G (p.Arg936Gly) n.2873A>G c.116-6332A>G (n.116-6332A>G) n.3044A>G c.2404A>G (p.Arg802Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.40622992A= | CA2171864183 | KNL1 | c.2728A= (p.Arg910=) c.2806A= (p.Arg936=) n.2873A= c.116-6332A= (n.116-6332A=) n.3044A= c.2404A= (p.Arg802=) | dbSNP |