Colon Cancer: Gene >> ARRB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269260
Start	4717911:4717911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758418471
CDS Mutation	c.509G>A
AA Mutation	p.Arg170Gln(p.R170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269260
Start	4717968:4717968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373133862
CDS Mutation	c.566G>A
AA Mutation	p.Arg189His(p.R189H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269260
Start	4721012:4721012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269260
Start	4716515:4716515(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.269delC
AA Mutation	p.Pro90ArgfsTer17(p.P90Rfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ARRB2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269260
Start	4718299:4718299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754430222
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript