Colon Cancer: Gene >> TIGIT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383671
Start	114295845:114295845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>T
AA Mutation	p.Arg121Ile(p.R121I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383671
Start	114295839:114295839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356C>G
AA Mutation	p.Thr119Ser(p.T119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383671
Start	114308081:114308081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685C>A
AA Mutation	p.Leu229Met(p.L229M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383671
Start	114295734:114295734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251G>A
AA Mutation	p.Arg84Gln(p.R84Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383671
Start	114295786:114295786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750866538
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000383671
Start	114295670:114295678(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.187_195delGACCAGCTT
AA Mutation	p.Asp63_Leu65del(p.D63_L65del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TIGIT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383671
Start	114294065:114294065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4C>A
AA Mutation	p.Arg2Ser(p.R2S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383671
Start	114295793:114295793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>T
AA Mutation	p.Gly104Trp(p.G104W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript