Colon Cancer: Gene >> CTSE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358184
Start	206012400:206012400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>C
AA Mutation	p.Val312Leu(p.V312L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358184
Start	206023737:206023737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.55G>A
AA Mutation	p.Gly19Arg(p.G19R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358184
Start	206021115:206021115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.396T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358184
Start	206015996:206015996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358184
Start	206022955:206022955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.171C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358184
Start	206016050:206016050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358184
Start	206012616:206012616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358184
Start	206012313:206012313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1021delC
AA Mutation	p.Leu341TyrfsTer71(p.L341Yfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CTSE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358184
Start	206021060:206021060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>A
AA Mutation	p.Asp151Asn(p.D151N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358184
Start	206021163:206021163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348G>T
Mutation Classification	Silent
Feature Type	Transcript