Colon Cancer: Gene >> UPRT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373383
Start	75293504:75293504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419C>T
AA Mutation	p.Ala140Val(p.A140V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373383
Start	75299864:75299864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>A
AA Mutation	p.Arg231Gln(p.R231Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373383
Start	75299888:75299888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.716C>T
AA Mutation	p.Pro239Leu(p.P239L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373383
Start	75293505:75293505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772176065
CDS Mutation	c.420G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373383
Start	75274503:75274503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373383
Start	75274372:75274372(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.122delG
AA Mutation	p.Gly41GlufsTer9(p.G41Efs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373383
Start	75299847:75299847(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.680delC
AA Mutation	p.Pro227GlnfsTer10(p.P227Qfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000373383
Start	75296387:75296387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475G>T
AA Mutation	p.Glu159Ter(p.E159*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000373383
Start	75299779:75299779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368655148
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Ter(p.R203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_lost
Transcription ID	ENST00000373383
Start	75303509:75303509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.928T>A
AA Mutation	p.Ter310LysextTer3(p.*310Kext*3)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> UPRT

No Mutation Annotation!