Colon Cancer: Gene >> TNFSF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223795
Start	114904081:114904081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.555C>G
AA Mutation	p.His185Gln(p.H185Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223795
Start	114905863:114905863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275G>A
AA Mutation	p.Arg92Lys(p.R92K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223795
Start	114905858:114905858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280C>A
AA Mutation	p.Pro94Thr(p.P94T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223795
Start	114904080:114904080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145748228
CDS Mutation	c.556G>A
AA Mutation	p.Val186Ile(p.V186I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000223795
Start	114904125:114904126(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.510dupA
AA Mutation	p.Gln171ThrfsTer8(p.Q171Tfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TNFSF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223795
Start	114930236:114930236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68C>T
AA Mutation	p.Pro23Leu(p.P23L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223795
Start	114930148:114930148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223795
Start	114904087:114904087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373154083
CDS Mutation	c.549G>A
Mutation Classification	Silent
Feature Type	Transcript