Colon Cancer: Gene >> DES

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373960
Start	219420576:219420576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770258461
CDS Mutation	c.817G>A
AA Mutation	p.Ala273Thr(p.A273T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373960
Start	219418584:219418584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122G>T
AA Mutation	p.Gly41Val(p.G41V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373960
Start	219420540:219420540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781G>T
AA Mutation	p.Val261Leu(p.V261L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373960
Start	219420275:219420275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374687448
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373960
Start	219421365:219421365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs57965306
CDS Mutation	c.1049G>A
AA Mutation	p.Arg350Gln(p.R350Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373960
Start	219418695:219418695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.233G>A
AA Mutation	p.Arg78His(p.R78H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373960
Start	219420321:219420321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374144840
CDS Mutation	c.710C>T
AA Mutation	p.Ala237Val(p.A237V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373960
Start	219420911:219420911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373960
Start	219420310:219420310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758066814
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000373960
Start	219420156:219420156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DES

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373960
Start	219420873:219420873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748742357
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Cys(p.R315C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373960
Start	219420320:219420320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397516697
CDS Mutation	c.709G>A
AA Mutation	p.Ala237Thr(p.A237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript