Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.43126651C>T | CA009200 | RET | c.2720C>T (p.Pro907Leu) n.2690C>T c.3116C>T (p.Pro1039Leu) c.*1710C>T (n.*1710C>T) c.*465C>T (n.*465C>T) c.2354C>T (p.Pro785Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.43126651C>A | CA009192 | RET | c.2720C>A (p.Pro907Gln) n.2690C>A c.3116C>A (p.Pro1039Gln) c.*1710C>A (n.*1710C>A) c.*465C>A (n.*465C>A) c.2354C>A (p.Pro785Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.43126651C>G | CA376558427 | RET | c.2720C>G (p.Pro907Arg) n.2690C>G c.3116C>G (p.Pro1039Arg) c.*1710C>G (n.*1710C>G) c.*465C>G (n.*465C>G) c.2354C>G (p.Pro785Arg) | ClinVar dbSNP |
10 | g.43126651C= | CA1905828751 | RET | c.2720C= (p.Pro907=) n.2690C= c.3116C= (p.Pro1039=) c.*1710C= (n.*1710C=) c.*465C= (n.*465C=) c.2354C= (p.Pro785=) | dbSNP |