Colon Cancer: Gene >> FBXO9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244426
Start	53097807:53097807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321G>A
AA Mutation	p.Ala441Thr(p.A441T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000244426
Start	53097786:53097786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1300G>A
AA Mutation	p.Ala434Thr(p.A434T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000244426
Start	53093466:53093466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894G>T
AA Mutation	p.Arg298Ser(p.R298S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000244426
Start	53092446:53092446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760965873
CDS Mutation	c.701G>A
AA Mutation	p.Arg234His(p.R234H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000244426
Start	53071090:53071090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67G>T
AA Mutation	p.Val23Phe(p.V23F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000244426
Start	53071056:53071056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33G>T
AA Mutation	p.Gln11His(p.Q11H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000244426
Start	53071054:53071054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31C>T
AA Mutation	p.Gln11Ter(p.Q11*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000244426
Start	53073624:53073625(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.264_265insCATTTTA
AA Mutation	p.Ala89HisfsTer26(p.A89Hfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FBXO9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000244426
Start	53093898:53093898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003C>A
AA Mutation	p.Leu335Ile(p.L335I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000244426
Start	53078890:53078890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429A>G
Mutation Classification	Silent
Feature Type	Transcript