Colon Cancer: Gene >> CYSLTR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282018
Start	48707593:48707593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776G>A
AA Mutation	p.Cys259Tyr(p.C259Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282018
Start	48707086:48707086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147650408
CDS Mutation	c.269C>T
AA Mutation	p.Thr90Met(p.T90M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282018
Start	48707159:48707159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342G>T
AA Mutation	p.Met114Ile(p.M114I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282018
Start	48707633:48707633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776586024
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYSLTR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282018
Start	48707532:48707532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201815757
CDS Mutation	c.715C>T
AA Mutation	p.Arg239Trp(p.R239W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282018
Start	48707658:48707658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>T
AA Mutation	p.Asp281Tyr(p.D281Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript