Colon Cancer: Gene >> TNFRSF17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000053243
Start	11966251:11966251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187A>G
AA Mutation	p.Ser63Gly(p.S63G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000053243
Start	11966253:11966253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189C>A
AA Mutation	p.Ser63Arg(p.S63R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000053243
Start	11965440:11965440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.116G>A
AA Mutation	p.Arg39His(p.R39H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000053243
Start	11967768:11967768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755751031
CDS Mutation	c.476C>T
AA Mutation	p.Thr159Met(p.T159M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000053243
Start	11966220:11966220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749544407
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000053243
Start	11966286:11966287(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.227dupT
AA Mutation	p.Leu76PhefsTer8(p.L76Ffs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000053243
Start	11966334:11966334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270A>C
AA Mutation	p.Lys90Asn(p.K90N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript