Colon Cancer: Gene >> PBX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420696
Start	164821586:164821586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201029742
CDS Mutation	c.1160G>T
AA Mutation	p.Gly387Val(p.G387V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000420696
Start	164812020:164812020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Trp(p.R290W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000420696
Start	164792577:164792577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Val117Met(p.V117M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000420696
Start	164821591:164821591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541105414
CDS Mutation	c.1165G>A
AA Mutation	p.Ala389Thr(p.A389T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000420696
Start	164799802:164799802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614A>G
AA Mutation	p.His205Arg(p.H205R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420696
Start	164821542:164821542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420696
Start	164792525:164792525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000420696
Start	164563303:164563303(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.262delA
AA Mutation	p.Thr88GlnfsTer3(p.T88Qfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PBX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420696
Start	164812105:164812105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953C>T
AA Mutation	p.Ala318Val(p.A318V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript