Colon Cancer: Gene >> DDOST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375048
Start	20652959:20652959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006G>A
AA Mutation	p.Val336Met(p.V336M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375048
Start	20652914:20652914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773138274
CDS Mutation	c.1051G>A
AA Mutation	p.Asp351Asn(p.D351N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375048
Start	20655491:20655491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551C>T
AA Mutation	p.Pro184Leu(p.P184L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375048
Start	20660956:20660956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241G>T
AA Mutation	p.Asp81Tyr(p.D81Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375048
Start	20655493:20655493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375048
Start	20652915:20652915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190780604
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375048
Start	20652418:20652418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375048
Start	20652656:20652656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138561924
CDS Mutation	c.1186C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375048
Start	20661300:20661300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.102G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375048
Start	20652463:20652463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376894317
CDS Mutation	c.1287C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DDOST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375048
Start	20654239:20654239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829G>C
AA Mutation	p.Ala277Pro(p.A277P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript