Colon Cancer: Gene >> IL11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264563
Start	55368548:55368548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748079395
CDS Mutation	c.202G>A
AA Mutation	p.Gly68Arg(p.G68R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264563
Start	55366042:55366042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201003688
CDS Mutation	c.565G>A
AA Mutation	p.Val189Met(p.V189M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264563
Start	55368845:55368845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104C>A
AA Mutation	p.Pro35His(p.P35H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264563
Start	55368824:55368824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125C>T
AA Mutation	p.Thr42Ile(p.T42I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264563
Start	55368558:55368558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264563
Start	55366098:55366098(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.509delG
AA Mutation	p.Gly170AlafsTer14(p.G170Afs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264563
Start	55368862:55368863(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.86dupC
AA Mutation	p.Arg30SerfsTer38(p.R30Sfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IL11

No Mutation Annotation!