Colon Cancer: Gene >> IL31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377035
Start	122173882:122173882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127G>A
AA Mutation	p.Glu43Lys(p.E43K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377035
Start	122173921:122173921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763913368
CDS Mutation	c.88C>T
AA Mutation	p.Arg30Cys(p.R30C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377035
Start	122172694:122172694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376559865
CDS Mutation	c.213G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL31

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377035
Start	122172485:122172485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422C>A
AA Mutation	p.Ser141Tyr(p.S141Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377035
Start	122172678:122172678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142483430
CDS Mutation	c.229G>A
AA Mutation	p.Ala77Thr(p.A77T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377035
Start	122173862:122173862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141921768
CDS Mutation	c.147G>A
Mutation Classification	Silent
Feature Type	Transcript