Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.245686793C>T | CA1488339 | KIF26B | c.3810C>T (p.Asp1270=) c.2667C>T (p.Asp889=) n.1741C>T c.3372C>T (p.Asp1124=) c.3210C>T (p.Asp1070=) n.1715-3410G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.245686793C= | CA1139838696 | KIF26B | c.3810C= (p.Asp1270=) c.2667C= (p.Asp889=) n.1741C= c.3372C= (p.Asp1124=) c.3210C= (p.Asp1070=) n.1715-3410G= | dbSNP |