Colon Cancer: Gene >> IL11RA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318041
Start	34657050:34657050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.347C>A
AA Mutation	p.Pro116His(p.P116H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318041
Start	34659882:34659882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934T>C
AA Mutation	p.Trp312Arg(p.W312R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318041
Start	34659807:34659807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.859C>G
AA Mutation	p.Leu287Val(p.L287V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318041
Start	34658546:34658546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538108515
CDS Mutation	c.673C>T
AA Mutation	p.Arg225Trp(p.R225W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318041
Start	34660931:34660931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778702237
CDS Mutation	c.1247G>A
AA Mutation	p.Arg416His(p.R416H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318041
Start	34656808:34656808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318041
Start	34655306:34655306(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.92delG
AA Mutation	p.Gly31AlafsTer14(p.G31Afs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000318041
Start	34660936:34660936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1252G>T
AA Mutation	p.Gly418Ter(p.G418*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL11RA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318041
Start	34657081:34657081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>T
AA Mutation	p.Glu126Asp(p.E126D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript