Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.1293971C>T | CA170792 | TERT | c.915G>A (p.Ala305=) n.973G>A n.994G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.1293971C>G | CA443240052 | TERT | c.915G>C (p.Ala305=) n.973G>C n.994G>C | dbSNP gnomAD v4 |
5 | g.1293971C= | CA1522556501 | TERT | c.915G= (p.Ala305=) n.973G= n.994G= | dbSNP |
5 | g.1293971C>A | CA443240051 | TERT | c.915G>T (p.Ala305=) n.973G>T n.994G>T | ClinVar dbSNP gnomAD v4 |