Colon Cancer: Gene >> CES2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317091
Start	66943919:66943919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753837525
CDS Mutation	c.1766C>T
AA Mutation	p.Ala589Val(p.A589V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317091
Start	66940495:66940495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761698722
CDS Mutation	c.808C>T
AA Mutation	p.Arg270Cys(p.R270C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317091
Start	66940565:66940565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371064921
CDS Mutation	c.878C>T
AA Mutation	p.Ala293Val(p.A293V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317091
Start	66940586:66940586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145407778
CDS Mutation	c.899C>T
AA Mutation	p.Ser300Leu(p.S300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317091
Start	66941628:66941628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753679470
CDS Mutation	c.1230C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317091
Start	66942203:66942203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368901475
CDS Mutation	c.1428G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317091
Start	66940497:66940497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317091
Start	66940587:66940587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149179989
CDS Mutation	c.900G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317091
Start	66939286:66939286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776138874
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317091
Start	66942242:66942242(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1470delT
AA Mutation	p.Gln491SerfsTer27(p.Q491Sfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CES2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317091
Start	66940586:66940586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145407778
CDS Mutation	c.899C>T
AA Mutation	p.Ser300Leu(p.S300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript