Colon Cancer: Gene >> TTPA

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260116
Start	63065905:63065905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202136581
CDS Mutation	c.551C>T
AA Mutation	p.Thr184Met(p.T184M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260116
Start	63061331:63061331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758A>T
AA Mutation	p.Glu253Val(p.E253V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260116
Start	63066026:63066027(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.429_430insTACCGTAA
AA Mutation	p.Val144TyrfsTer7(p.V144Yfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000260116
Start	63066053:63066054(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.402_403insTATACATTTACC
AA Mutation	p.Arg134_Val135insTyrThrPheThr(p.R134_V135insYTFT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TTPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260116
Start	63061268:63061268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.821C>A
AA Mutation	p.Ser274Tyr(p.S274Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000260116
Start	63066056:63066056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121917851
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Ter(p.R134*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript