Colon Cancer: Gene >> OMP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000529803
Start	77103246:77103246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369572640
CDS Mutation	c.407G>A
AA Mutation	p.Arg136His(p.R136H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000529803
Start	77103203:77103203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782632842
CDS Mutation	c.364G>A
AA Mutation	p.Ala122Thr(p.A122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000529803
Start	77103174:77103174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782164015
CDS Mutation	c.335C>T
AA Mutation	p.Ser112Leu(p.S112L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529803
Start	77103091:77103091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371003394
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529803
Start	77103265:77103265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373450635
CDS Mutation	c.426C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OMP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000529803
Start	77103150:77103150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311C>A
AA Mutation	p.Ala104Asp(p.A104D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript