Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.74097222C>T | CA273521 | VCL | c.1762C>T (p.Gln588Ter) c.778C>T (p.Gln260Ter) n.332-3832C>T n.4565C>T c.*1517C>T (n.*1517C>T) c.1765C>T (p.Gln589Ter) | ClinVar dbSNP |
10 | g.74097222C= | CA1919890080 | VCL | c.1762C= (p.Gln588=) c.778C= (p.Gln260=) n.332-3832C= n.4565C= c.*1517C= (n.*1517C=) c.1765C= (p.Gln589=) | dbSNP |