Colon Cancer: Gene >> CD28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324106
Start	203734842:203734842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199647272
CDS Mutation	c.593G>A
AA Mutation	p.Arg198His(p.R198H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324106
Start	203726900:203726900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.320C>A
AA Mutation	p.Thr107Lys(p.T107K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324106
Start	203726751:203726751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171A>C
AA Mutation	p.Lys57Asn(p.K57N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324106
Start	203734888:203734888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142698532
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324106
Start	203726658:203726658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199844145
CDS Mutation	c.78G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324106
Start	203734894:203734894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324106
Start	203734835:203734835(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.589delC
AA Mutation	p.Arg197AlafsTer83(p.R197Afs*83)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CD28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324106
Start	203734889:203734889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201909740
CDS Mutation	c.640G>A
AA Mutation	p.Asp214Asn(p.D214N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript