Colon Cancer: Gene >> CD86

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330540
Start	122103812:122103812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775704428
CDS Mutation	c.365G>A
AA Mutation	p.Arg122His(p.R122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330540
Start	122119479:122119479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370380261
CDS Mutation	c.935G>A
AA Mutation	p.Arg312His(p.R312H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330540
Start	122103765:122103765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330540
Start	122106388:122106388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199853120
CDS Mutation	c.591C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330540
Start	122106337:122106337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780454711
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000330540
Start	122103726:122103726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279G>A
AA Mutation	p.Trp93Ter(p.W93*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000330540
Start	122106242:122106242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445G>T
AA Mutation	p.Glu149Ter(p.E149*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CD86

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330540
Start	122103631:122103631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184A>C
AA Mutation	p.Asn62His(p.N62H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330540
Start	122091646:122091646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60C>A
Mutation Classification	Silent
Feature Type	Transcript