Colon Cancer: Gene >> POU5F1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259915
Start	31165135:31165135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809A>G
AA Mutation	p.Glu270Gly(p.E270G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259915
Start	31164794:31164794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890A>G
AA Mutation	p.Asp297Gly(p.D297G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259915
Start	31165206:31165206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738G>T
AA Mutation	p.Glu246Asp(p.E246D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259915
Start	31170546:31170546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780177765
CDS Mutation	c.75G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259915
Start	31170427:31170427(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.194delC
AA Mutation	p.Pro65ArgfsTer20(p.P65Rfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259915
Start	31164723:31164724(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.960dupT
AA Mutation	p.Gly321TrpfsTer21(p.G321Wfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259915
Start	31170313:31170314(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.307dupG
AA Mutation	p.Val103GlyfsTer86(p.V103Gfs*86)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> POU5F1

Mutation ID	1
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000259915
Start	31164801:31164803(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs765569430
CDS Mutation	c.881_883delAAC
AA Mutation	p.Gln294del(p.Q294del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript