Colon Cancer: Gene >> TNFSF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245817
Start	6534653:6534653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352G>A
AA Mutation	p.Val118Met(p.V118M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245817
Start	6535040:6535040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2234180
CDS Mutation	c.739G>A
AA Mutation	p.Gly247Arg(p.G247R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245817
Start	6535028:6535028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778848855
CDS Mutation	c.727G>A
AA Mutation	p.Glu243Lys(p.E243K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245817
Start	6534752:6534752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750244943
CDS Mutation	c.451C>T
AA Mutation	p.Arg151Cys(p.R151C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245817
Start	6534691:6534691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245817
Start	6534664:6534664(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.368delG
AA Mutation	p.Gly123AlafsTer2(p.G123Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TNFSF9

No Mutation Annotation!