Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.3736690A>G | CA16603336 | CREBBP | c.4520T>C (p.Leu1507Pro) c.4406T>C (p.Leu1469Pro) c.3155T>C (p.Leu1052Pro) n.310T>C n.341T>C n.3343T>C c.4475T>C (p.Leu1492Pro) c.4103T>C (p.Leu1368Pro) c.4259T>C (p.Leu1420Pro) c.4466T>C (p.Leu1489Pro) c.3767T>C (p.Leu1256Pro) c.4514T>C (p.Leu1505Pro) | ClinVar dbSNP COSMIC |
16 | g.3736690A>T | CA394563476 | CREBBP | c.4520T>A (p.Leu1507Gln) c.4406T>A (p.Leu1469Gln) c.3155T>A (p.Leu1052Gln) n.310T>A n.341T>A n.3343T>A c.4475T>A (p.Leu1492Gln) c.4103T>A (p.Leu1368Gln) c.4259T>A (p.Leu1420Gln) c.4466T>A (p.Leu1489Gln) c.3767T>A (p.Leu1256Gln) c.4514T>A (p.Leu1505Gln) | dbSNP |