Colon Cancer: Gene >> PTX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295927
Start	157442506:157442506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673T>C
AA Mutation	p.Phe225Leu(p.F225L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295927
Start	157436984:157436984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295927
Start	157437613:157437613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000295927
Start	157442536:157442536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703G>T
AA Mutation	p.Glu235Ter(p.E235*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PTX3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295927
Start	157436948:157436948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15G>A
Mutation Classification	Silent
Feature Type	Transcript