Colon Cancer: Gene >> PLAUR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340093
Start	43649084:43649084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756038834
CDS Mutation	c.814G>A
AA Mutation	p.Ala272Thr(p.A272T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340093
Start	43656605:43656605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346G>A
AA Mutation	p.Glu116Lys(p.E116K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340093
Start	43656594:43656594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.357C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000340093
Start	43656527:43656527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424G>T
AA Mutation	p.Glu142Ter(p.E142*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PLAUR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340093
Start	43667629:43667629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118G>T
AA Mutation	p.Ala40Ser(p.A40S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340093
Start	43648914:43648914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984G>T
AA Mutation	p.Trp328Cys(p.W328C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript