Colon Cancer: Gene >> IL19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270218
Start	206839962:206839962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323C>T
AA Mutation	p.Ala108Val(p.A108V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340758
Start	206798911:206798911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17C>T
AA Mutation	p.Ala6Val(p.A6V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270218
Start	206841064:206841064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424G>A
AA Mutation	p.Asp142Asn(p.D142N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270218
Start	206839894:206839894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143520689
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270218
Start	206839868:206839868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375138273
CDS Mutation	c.229G>A
AA Mutation	p.Val77Met(p.V77M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270218
Start	206841043:206841043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403A>G
AA Mutation	p.Asn135Asp(p.N135D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript