Colon Cancer: Gene >> MIA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263369
Start	40775790:40775790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166G>A
AA Mutation	p.Ala56Thr(p.A56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263369
Start	40775796:40775796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>A
AA Mutation	p.Asp58Asn(p.D58N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263369
Start	40775549:40775549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371769033
CDS Mutation	c.7C>T
AA Mutation	p.Arg3Trp(p.R3W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263369
Start	40775756:40775756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263369
Start	40775626:40775627(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.86dupA
AA Mutation	p.Leu30AlafsTer3(p.L30Afs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000263369
Start	40776967:40776967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MIA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263369
Start	40775649:40775649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375928719
CDS Mutation	c.107G>A
AA Mutation	p.Cys36Tyr(p.C36Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263369
Start	40775567:40775567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25G>T
AA Mutation	p.Gly9Cys(p.G9C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript