Colon Cancer: Gene >> PBX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375050
Start	32188740:32188740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278A>G
AA Mutation	p.Glu93Gly(p.E93G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375050
Start	32186872:32186872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054T>G
AA Mutation	p.Ser352Ala(p.S352A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375050
Start	32187253:32187253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1013C>G
AA Mutation	p.Pro338Arg(p.P338R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375050
Start	32188736:32188736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375050
Start	32186837:32186837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147090639
CDS Mutation	c.1089C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375050
Start	32188349:32188350(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.450_451insGGAT
AA Mutation	p.Ser151GlyfsTer4(p.S151Gfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PBX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375050
Start	32188269:32188269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531G>T
AA Mutation	p.Glu177Asp(p.E177D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript