Colon Cancer: Gene >> S1PR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000590320
Start	10224484:10224484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Gly141Asp(p.G141D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000590320
Start	10224419:10224419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487G>A
AA Mutation	p.Gly163Ser(p.G163S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000590320
Start	10224808:10224808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98G>A
AA Mutation	p.Arg33His(p.R33H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590320
Start	10224816:10224816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776010598
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> S1PR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000590320
Start	10224647:10224647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759886451
CDS Mutation	c.259G>A
AA Mutation	p.Val87Ile(p.V87I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript