Colon Cancer: Gene >> IL32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396890
Start	3069039:3069039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371449782
CDS Mutation	c.389G>A
AA Mutation	p.Gly130Asp(p.G130D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396890
Start	3068214:3068214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314C>T
AA Mutation	p.Ala105Val(p.A105V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396890
Start	3069161:3069161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538977484
CDS Mutation	c.511G>A
AA Mutation	p.Gly171Arg(p.G171R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396890
Start	3069288:3069288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638G>A
AA Mutation	p.Gly213Glu(p.G213E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL32

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396890
Start	3069324:3069324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674A>G
AA Mutation	p.Gln225Arg(p.Q225R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript