Colon Cancer: Gene >> BCAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270233
Start	44814182:44814182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815G>A
AA Mutation	p.Gly272Asp(p.G272D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270233
Start	44813551:44813551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772105916
CDS Mutation	c.715G>A
AA Mutation	p.Ala239Thr(p.A239T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270233
Start	44812385:44812385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778465310
CDS Mutation	c.427G>A
AA Mutation	p.Val143Met(p.V143M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270233
Start	44819077:44819077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766822712
CDS Mutation	c.1358C>T
AA Mutation	p.Ala453Val(p.A453V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270233
Start	44819121:44819121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569668745
CDS Mutation	c.1402G>A
AA Mutation	p.Glu468Lys(p.E468K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270233
Start	44819467:44819467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140735488
CDS Mutation	c.1595G>A
AA Mutation	p.Arg532His(p.R532H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270233
Start	44819686:44819686(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1727delG
AA Mutation	p.Gly576AlafsTer20(p.G576Afs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000270233
Start	44812506:44812507(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.464dupA
AA Mutation	p.Asn155LysfsTer76(p.N155Kfs*76)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BCAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270233
Start	44814272:44814272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768582759
CDS Mutation	c.905C>T
AA Mutation	p.Thr302Met(p.T302M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270233
Start	44814262:44814262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895C>T
AA Mutation	p.Pro299Ser(p.P299S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript