Colon Cancer: Gene >> TNFRSF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377507
Start	7935057:7935057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145966863
CDS Mutation	c.500C>T
AA Mutation	p.Pro167Leu(p.P167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377507
Start	7933216:7933216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777956091
CDS Mutation	c.625C>T
AA Mutation	p.Arg209Cys(p.R209C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377507
Start	7937749:7937749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.354A>C
AA Mutation	p.Lys118Asn(p.K118N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377507
Start	7939926:7939926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756511571
CDS Mutation	c.69A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377507
Start	7933187:7933187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.654G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377507
Start	7933187:7933187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.654G>T
AA Mutation	p.Lys218Asn(p.K218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377507
Start	7933286:7933286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript