Colon Cancer: Gene >> PANX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000227638
Start	94153533:94153533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>A
AA Mutation	p.Arg75His(p.R75H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000227638
Start	94178564:94178564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517C>T
AA Mutation	p.Pro173Ser(p.P173S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227638
Start	94179727:94179743(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.674_690delTGTTAGCGTGTATCTAC
AA Mutation	p.Leu225ProfsTer50(p.L225Pfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000227638
Start	94129448:94129448(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.139delC
AA Mutation	p.Leu47CysfsTer18(p.L47Cfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000227638
Start	94179740:94179740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684T>A
AA Mutation	p.Cys228Ter(p.C228*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000227638
Start	94129397:94129397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Ter(p.R29*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PANX1

No Mutation Annotation!