Colon Cancer: Gene >> TNFRSF18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379268
Start	1204075:1204075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.560T>C
AA Mutation	p.Leu187Pro(p.L187P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379268
Start	1204232:1204232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403A>G
AA Mutation	p.Thr135Ala(p.T135A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379268
Start	1206431:1206431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379268
Start	1204434:1204434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542243245
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF18

No Mutation Annotation!