Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.149378166C>A | CA16042629 | TAB2 | n.666C>A c.251C>A (p.Ser84Ter) c.-96-506C>A (n.-96-506C>A) c.29C>A (p.Ser10Ter) c.155C>A (p.Ser52Ter) | ClinVar dbSNP |
6 | g.149378166C>T | CA365993159 | TAB2 | n.666C>T c.251C>T (p.Ser84Leu) c.-96-506C>T (n.-96-506C>T) c.29C>T (p.Ser10Leu) c.155C>T (p.Ser52Leu) | ClinVar dbSNP |
6 | g.149378166C= | CA1671914789 | TAB2 | n.666C= c.251C= (p.Ser84=) c.-96-506C= (n.-96-506C=) c.29C= (p.Ser10=) c.155C= (p.Ser52=) | dbSNP |