Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BMX

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000342014
Start 15522481:15522481(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.646T>C
AA Mutation p.Tyr216His(p.Y216H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000342014
Start 15508367:15508367(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.14C>A
AA Mutation p.Ser5Tyr(p.S5Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000342014
Start 15509405:15509405(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774703027
CDS Mutation c.215C>T
AA Mutation p.Thr72Met(p.T72M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000342014
Start 15522432:15522432(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.597G>T
AA Mutation p.Lys199Asn(p.K199N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000342014
Start 15549887:15549887(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1843T>G
AA Mutation p.Leu615Val(p.L615V)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> BMX

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000342014
Start 15509333:15509333(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763057245
CDS Mutation c.143G>A
AA Mutation p.Arg48Lys(p.R48K)
Mutation Classification Missense_Mutation
Feature Type Transcript