Colon Cancer: Gene >> PLAU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372764
Start	73915371:73915371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091A>G
AA Mutation	p.Asp364Gly(p.D364G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372764
Start	73913367:73913367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446A>G
AA Mutation	p.His149Arg(p.H149R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372764
Start	73916456:73916456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187G>T
AA Mutation	p.Trp396Leu(p.W396L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372764
Start	73916491:73916491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200165551
CDS Mutation	c.1222G>A
AA Mutation	p.Val408Ile(p.V408I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372764
Start	73913660:73913660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760979977
CDS Mutation	c.582G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372764
Start	73912300:73912300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375409521
CDS Mutation	c.171C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000372764
Start	73913625:73913625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547G>T
AA Mutation	p.Glu183Ter(p.E183*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PLAU

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372764
Start	73912300:73912300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375409521
CDS Mutation	c.171C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000372764
Start	73913625:73913625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547G>T
AA Mutation	p.Glu183Ter(p.E183*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript