Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> S1PR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89001388:89001388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188C>T
AA Mutation	p.Ala63Val(p.A63V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89002333:89002333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1133A>G
AA Mutation	p.Asn378Ser(p.N378S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89002009:89002009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809G>T
AA Mutation	p.Arg270Met(p.R270M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358157
Start	89002172:89002172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201820975
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358157
Start	89001368:89001368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577646307
CDS Mutation	c.168G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358157
Start	89001344:89001344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358157
Start	89001557:89001557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> S1PR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89002225:89002225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1025G>A
AA Mutation	p.Ser342Asn(p.S342N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89002053:89002053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778339232
CDS Mutation	c.853G>A
AA Mutation	p.Val285Met(p.V285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358157
Start	89002049:89002049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849C>A
AA Mutation	p.Phe283Leu(p.F283L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358157
Start	89001707:89001707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript