Colon Cancer: Gene >> NFKBIZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326172
Start	101853239:101853239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713G>T
AA Mutation	p.Ser238Ile(p.S238I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326172
Start	101855084:101855084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1466C>T
AA Mutation	p.Ala489Val(p.A489V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326172
Start	101855203:101855203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1585C>T
AA Mutation	p.Leu529Phe(p.L529F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326172
Start	101852986:101852986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561T>G
AA Mutation	p.Phe187Leu(p.F187L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326172
Start	101857444:101857444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2088C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326172
Start	101853153:101853154(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.628dupC
AA Mutation	p.Gln210ProfsTer6(p.Q210Pfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NFKBIZ

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326172
Start	101859360:101859360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2146C>T
AA Mutation	p.Pro716Ser(p.P716S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326172
Start	101853458:101853458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.932G>A
AA Mutation	p.Ser311Asn(p.S311N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript