Colon Cancer: Gene >> POU5F1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000465342
Start	127416891:127416891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1025A>G
AA Mutation	p.Glu342Gly(p.E342G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000465342
Start	127416653:127416653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.787G>A
AA Mutation	p.Ala263Thr(p.A263T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000465342
Start	127415940:127415940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74C>T
AA Mutation	p.Ala25Val(p.A25V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465342
Start	127416304:127416304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465342
Start	127416685:127416685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000465342
Start	127416054:127416055(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.194dupC
AA Mutation	p.Pro66AlafsTer3(p.P66Afs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000465342
Start	127416216:127416217(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.356dupC
AA Mutation	p.Gly120TrpfsTer69(p.G120Wfs*69)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> POU5F1B

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465342
Start	127416028:127416028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000465342
Start	127416566:127416566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Ter(p.R234*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript