Colon Cancer: Gene >> MXI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000239007
Start	110284905:110284905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605T>A
AA Mutation	p.Ile202Asn(p.I202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000239007
Start	110228206:110228206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91G>A
AA Mutation	p.Ala31Thr(p.A31T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000239007
Start	110280026:110280026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367591565
CDS Mutation	c.464G>A
AA Mutation	p.Arg155Gln(p.R155Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000239007
Start	110284911:110284911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611A>G
AA Mutation	p.Asp204Gly(p.D204G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239007
Start	110228220:110228220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MXI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000239007
Start	110279933:110279933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>T
AA Mutation	p.Arg124Ile(p.R124I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000239007
Start	110280026:110280026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367591565
CDS Mutation	c.464G>A
AA Mutation	p.Arg155Gln(p.R155Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript