Colon Cancer: Gene >> CST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304749
Start	23749106:23749106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.252C>A
AA Mutation	p.Phe84Leu(p.F84L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304749
Start	23750717:23750717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566215865
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304749
Start	23749103:23749103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769607319
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304749
Start	23749117:23749117(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs781037716
CDS Mutation	c.241delG
AA Mutation	p.Val81Ter(p.V81*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304749
Start	23750662:23750662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768059525
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Trp(p.R69W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript