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1 protein found in SwissVar (37 variants)

with gene/protein name P15056

Disclaimer: The query results are intended for research purposes only, not for clinical and diagnostic use.

Accession Entry name Disease Variants 3D mapping
(variant position)
P15056 BRAF_HUMAN wide range of cancers
P15056 BRAF_HUMAN colorectal cancer p.Arg462Ile
p.Ile463Ser
p.Gly464Val
p.Gly464Glu
p.Val600Glu
p.Lys601Glu






P15056 BRAF_HUMAN lung cancer p.Gly466Val
p.Leu597Arg


P15056 BRAF_HUMAN familial non-hodgkin lymphoma p.Gly469Ala
p.Gly469Arg
p.Asp594Gly



P15056 BRAF_HUMAN cardiofaciocutaneous syndrome 1 p.Thr241Pro
p.Thr244Pro
p.Leu245Phe
p.Ala246Pro
p.Gln257Arg
p.Gln262Lys
p.Glu275Lys
p.Ser467Ala
p.Phe468Ser
p.Gly469Glu
p.Leu485Phe
p.Lys499Glu
p.Lys499Asn
p.Glu501Lys
p.Glu501Gly
p.Leu525Pro
p.Asn580Asp
p.Asn581Asp
p.Phe595Leu
p.Gly596Val
p.Thr599Arg
p.Lys601Gln
p.Asp638Glu
p.Gln709Arg
























P15056 BRAF_HUMAN noonan syndrome 7 p.Trp531Cys
p.Leu597Val


P15056 BRAF_HUMAN leopard syndrome 3 p.Thr241Pro

P15056 BRAF_HUMAN pilocytic astrocytomas