Colon Cancer: Gene >> ASL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304874
Start	66086754:66086754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.535G>A
AA Mutation	p.Ala179Thr(p.A179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304874
Start	66089162:66089162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758359461
CDS Mutation	c.905G>A
AA Mutation	p.Arg302His(p.R302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304874
Start	66089313:66089313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774195710
CDS Mutation	c.956G>A
AA Mutation	p.Ser319Asn(p.S319N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304874
Start	66092842:66092842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1325G>A
AA Mutation	p.Gly442Asp(p.G442D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ASL

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304874
Start	66086747:66086747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150557376
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304874
Start	66083127:66083127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141584041
CDS Mutation	c.399G>A
Mutation Classification	Silent
Feature Type	Transcript