Colon Cancer: Gene >> CST7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000480798
Start	24958931:24958931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771107712
CDS Mutation	c.247G>A
AA Mutation	p.Val83Met(p.V83M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000480798
Start	24959000:24959000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371415469
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Cys(p.R106C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000480798
Start	24949569:24949570(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.68dupC
AA Mutation	p.Asp24ArgfsTer8(p.D24Rfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CST7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000480798
Start	24957337:24957337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.121A>G
AA Mutation	p.Thr41Ala(p.T41A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript