Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> YAP1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282441
Start 102206045:102206045(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754280015
CDS Mutation c.955C>T
AA Mutation p.Arg319Trp(p.R319W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000282441
Start 102186114:102186114(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.785G>T
AA Mutation p.Arg262Met(p.R262M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000282441
Start 102114185:102114185(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.363G>T
AA Mutation p.Gln121His(p.Q121H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000282441
Start 102114185:102114185(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.363G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence inframe_insertion
Transcription ID ENST00000282441
Start 102229859:102229860(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1434_1435insGTTGAT
AA Mutation p.Leu478_Ser479insValAsp(p.L478_S479insVD)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> YAP1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000282441
Start 102114235:102114235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.413C>T
AA Mutation p.Ser138Phe(p.S138F)
Mutation Classification Missense_Mutation
Feature Type Transcript