Colon Cancer: Gene >> IL3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000296870
Start	132062670:132062670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758836570
CDS Mutation	c.338G>A
AA Mutation	p.Arg113Gln(p.R113Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296870
Start	132062554:132062554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546686029
CDS Mutation	c.323C>T
AA Mutation	p.Thr108Met(p.T108M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296870
Start	132062375:132062375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761206378
CDS Mutation	c.268G>A
AA Mutation	p.Ala90Thr(p.A90T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296870
Start	132062785:132062785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296870
Start	132060721:132060721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373333851
CDS Mutation	c.15C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296870
Start	132062725:132062725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750120195
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IL3

Mutation ID	1
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000296870
Start	132062568:132062568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript