Colon Cancer: Gene >> CD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000011653
Start	6814974:6814974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589A>G
AA Mutation	p.Ile197Val(p.I197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000011653
Start	6814196:6814196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269G>A
AA Mutation	p.Gly90Glu(p.G90E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000011653
Start	6816252:6816252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804G>T
AA Mutation	p.Gln268His(p.Q268H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000011653
Start	6816283:6816283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.835C>T
AA Mutation	p.Pro279Ser(p.P279S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011653
Start	6800422:6800422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011653
Start	6818476:6818476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782144509
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000011653
Start	6814877:6814877(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.498delG
AA Mutation	p.Lys167ArgfsTer31(p.K167Rfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000011653
Start	6817308:6817309(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1134_1135insAAATTTTT
AA Mutation	p.Leu379LysfsTer24(p.L379Kfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000011653
Start	6816086:6816086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638A>C
AA Mutation	p.Lys213Thr(p.K213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript