Colon Cancer: Gene >> ASB9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380488
Start	15250511:15250511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487A>G
AA Mutation	p.Lys163Glu(p.K163E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380488
Start	15248875:15248875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629C>G
AA Mutation	p.Ala210Gly(p.A210G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380488
Start	15254822:15254822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.197C>T
AA Mutation	p.Thr66Met(p.T66M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380488
Start	15269813:15269813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.62G>A
AA Mutation	p.Gly21Asp(p.G21D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380488
Start	15248814:15248814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ASB9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380488
Start	15248932:15248932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572C>T
AA Mutation	p.Ala191Val(p.A191V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript