Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.3736690A>GCA16603336CREBBPc.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
16g.3736690A>TCA394563476CREBBPc.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

Number of alleles fetched