Colon Cancer: Gene >> BEX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372728
Start	103063111:103063111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164T>C
AA Mutation	p.Val55Ala(p.V55A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372728
Start	103063121:103063121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154C>T
AA Mutation	p.Arg52Trp(p.R52W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372728
Start	103063225:103063225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1045065
CDS Mutation	c.50C>T
AA Mutation	p.Ala17Val(p.A17V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372728
Start	103062973:103062973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302T>C
AA Mutation	p.Leu101Ser(p.L101S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372728
Start	103062937:103062937(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.338delC
AA Mutation	p.Pro113LeufsTer16(p.P113Lfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BEX1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000372728
Start	103063262:103063262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13G>T
AA Mutation	p.Glu5Ter(p.E5*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript