Colon Cancer: Gene >> PFKFB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379775
Start	6220693:6220693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140784797
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379775
Start	6226315:6226315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750254792
CDS Mutation	c.1465G>A
AA Mutation	p.Ala489Thr(p.A489T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379775
Start	6220791:6220791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379775
Start	6222878:6222878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379775
Start	6224195:6224195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1323A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379775
Start	6219580:6219580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379775
Start	6224007:6224007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771030415
CDS Mutation	c.1263G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PFKFB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379775
Start	6219657:6219657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587C>A
AA Mutation	p.Ala196Asp(p.A196D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379775
Start	6222942:6222942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1171G>C
AA Mutation	p.Val391Leu(p.V391L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379775
Start	6216764:6216764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425A>C
AA Mutation	p.Lys142Thr(p.K142T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379775
Start	6215231:6215231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374201933
CDS Mutation	c.213C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000379775
Start	6223957:6223957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1214-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript