Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SULT1E1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69842051:69842051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828T>A
AA Mutation	p.Asp276Glu(p.D276E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69855328:69855328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244G>C
AA Mutation	p.Glu82Gln(p.E82Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69844170:69844170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763A>G
AA Mutation	p.Met255Val(p.M255V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69849510:69849510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423C>A
AA Mutation	p.Phe141Leu(p.F141L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69854287:69854287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299C>A
AA Mutation	p.Ser100Tyr(p.S100Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69857523:69857523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122T>C
AA Mutation	p.Val41Ala(p.V41A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226444
Start	69844309:69844309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226444
Start	69855392:69855392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SULT1E1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69844304:69844304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629T>C
AA Mutation	p.Leu210Pro(p.L210P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69854287:69854287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299C>A
AA Mutation	p.Ser100Tyr(p.S100Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69842055:69842055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824T>G
AA Mutation	p.Phe275Cys(p.F275C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226444
Start	69844241:69844241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692T>C
AA Mutation	p.Met231Thr(p.M231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript