| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.152326137G>T | CA16602862 | FBXW7 | c.*206C>A (n.*206C>A) c.1012C>A (p.Arg338Ser) c.1513C>A (p.Arg505Ser) c.*1160C>A (n.*1160C>A) c.*489C>A (n.*489C>A) c.1159C>A (p.Arg387Ser) c.1273C>A (p.Arg425Ser) n.1062C>A c.985C>A (p.Arg329Ser) n.961C>A c.1429C>A (p.Arg477Ser) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 4 | g.152326137G>C | CA16602859 | FBXW7 | c.*206C>G (n.*206C>G) c.1012C>G (p.Arg338Gly) c.1513C>G (p.Arg505Gly) c.*1160C>G (n.*1160C>G) c.*489C>G (n.*489C>G) c.1159C>G (p.Arg387Gly) c.1273C>G (p.Arg425Gly) n.1062C>G c.985C>G (p.Arg329Gly) n.961C>G c.1429C>G (p.Arg477Gly) | ClinVar dbSNP COSMIC COSMIC COSMIC COSMIC COSMIC |
| 4 | g.152326137G>A | CA16602253 | FBXW7 | c.*206C>T (n.*206C>T) c.1012C>T (p.Arg338Cys) c.1513C>T (p.Arg505Cys) c.*1160C>T (n.*1160C>T) c.*489C>T (n.*489C>T) c.1159C>T (p.Arg387Cys) c.1273C>T (p.Arg425Cys) n.1062C>T c.985C>T (p.Arg329Cys) n.961C>T c.1429C>T (p.Arg477Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC COSMIC COSMIC |