Colon Cancer: Gene >> POGLUT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295588
Start	119490625:119490625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.872T>C
AA Mutation	p.Phe291Ser(p.F291S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295588
Start	119480078:119480078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484C>T
AA Mutation	p.Pro162Ser(p.P162S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295588
Start	119469838:119469838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104T>G
AA Mutation	p.Phe35Cys(p.F35C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295588
Start	119491530:119491530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200054647
CDS Mutation	c.978A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295588
Start	119490555:119490555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000295588
Start	119491517:119491517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> POGLUT1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295588
Start	119486911:119486911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript