Colon Cancer: Gene >> S1PR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239783:101239783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528925521
CDS Mutation	c.799G>A
AA Mutation	p.Ala267Thr(p.A267T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239407:101239407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423G>T
AA Mutation	p.Glu141Asp(p.E141D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239564:101239564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580G>A
AA Mutation	p.Val194Met(p.V194M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239997:101239997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1013G>A
AA Mutation	p.Gly338Asp(p.G338D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239756:101239756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>A
AA Mutation	p.Val258Ile(p.V258I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239649:101239649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.665G>A
AA Mutation	p.Cys222Tyr(p.C222Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239939:101239939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955C>T
AA Mutation	p.Arg319Cys(p.R319C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239979:101239979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995C>T
AA Mutation	p.Pro332Leu(p.P332L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239408:101239408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Cys(p.R142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305352
Start	101239212:101239212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305352
Start	101239644:101239644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305352
Start	101239863:101239863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764924903
CDS Mutation	c.879G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> S1PR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101240116:101240116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769569528
CDS Mutation	c.1132G>A
AA Mutation	p.Val378Ile(p.V378I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239474:101239474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490A>G
AA Mutation	p.Ile164Val(p.I164V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305352
Start	101239935:101239935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.951G>T
AA Mutation	p.Glu317Asp(p.E317D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript