Colon Cancer: Gene >> PBX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373489
Start	125965907:125965907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1289C>T
AA Mutation	p.Ser430Leu(p.S430L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373489
Start	125929842:125929842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704C>T
AA Mutation	p.Ala235Val(p.A235V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373489
Start	125963024:125963024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778017986
CDS Mutation	c.1135C>T
AA Mutation	p.Arg379Cys(p.R379C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373489
Start	125915761:125915761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350C>T
AA Mutation	p.Ala117Val(p.A117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373489
Start	125935486:125935486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722A>G
AA Mutation	p.Asn241Ser(p.N241S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373489
Start	125748586:125748586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373489
Start	125747540:125747540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000373489
Start	125929760:125929760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Ter(p.R208*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000373489
Start	125963103:125963103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PBX3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373489
Start	125962150:125962150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1058A>G
AA Mutation	p.Asn353Ser(p.N353S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript