Colon Cancer: Gene >> MRO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256425
Start	50801428:50801428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506A>C
AA Mutation	p.Lys169Thr(p.K169T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256425
Start	50801426:50801426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141296827
CDS Mutation	c.508T>A
AA Mutation	p.Phe170Ile(p.F170I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256425
Start	50806722:50806722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569083454
CDS Mutation	c.228C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256425
Start	50801499:50801499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557582477
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256425
Start	50806770:50806770(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.180delC
AA Mutation	p.Ser61ValfsTer9(p.S61Vfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000256425
Start	50805153:50805153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372190392
CDS Mutation	c.429+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MRO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256425
Start	50806756:50806756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370546021
CDS Mutation	c.194G>A
AA Mutation	p.Arg65His(p.R65H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript