Colon Cancer: Gene >> GPS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380728
Start	7313115:7313115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192050225
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380728
Start	7314357:7314357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251A>G
AA Mutation	p.His84Arg(p.H84R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000380728
Start	7313907:7313907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760303804
CDS Mutation	c.479C>T
AA Mutation	p.Thr160Met(p.T160M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380728
Start	7314583:7314583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109G>A
AA Mutation	p.Asp37Asn(p.D37N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380728
Start	7313671:7313671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000380728
Start	7313049:7313049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.880C>T
AA Mutation	p.Gln294Ter(p.Q294*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GPS2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000380728
Start	7314304:7314304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304C>T
AA Mutation	p.Arg102Ter(p.R102*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript