Colon Cancer: Gene >> SP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375281
Start	170717222:170717222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Cys(p.R339C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375281
Start	170716903:170716903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375281
Start	170716466:170716466(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.263delC
AA Mutation	p.Pro88ArgfsTer7(p.P88Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375281
Start	170716991:170716992(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.790dupC
AA Mutation	p.Leu264ProfsTer118(p.L264Pfs*118)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375281
Start	170717117:170717117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779921916
CDS Mutation	c.910G>A
AA Mutation	p.Gly304Ser(p.G304S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript