Colon Cancer: Gene >> TAPBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000426633
Start	33304188:33304188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749133011
CDS Mutation	c.1240G>A
AA Mutation	p.Val414Ile(p.V414I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000426633
Start	33304547:33304547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.960C>A
AA Mutation	p.Phe320Leu(p.F320L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426633
Start	33304415:33304415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426633
Start	33305152:33305152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000426633
Start	33305296:33305296(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.561delC
AA Mutation	p.Thr188ProfsTer17(p.T188Pfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000426633
Start	33304463:33304463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1044G>A
AA Mutation	p.Trp348Ter(p.W348*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TAPBP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000426633
Start	33304359:33304359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750940622
CDS Mutation	c.1148G>A
AA Mutation	p.Arg383Gln(p.R383Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000426633
Start	33304428:33304428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1079T>C
AA Mutation	p.Val360Ala(p.V360A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript