Colon Cancer: Gene >> ACOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301608
Start	75955661:75955661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.679G>A
AA Mutation	p.Gly227Ser(p.G227S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301608
Start	75949284:75949284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1661T>A
AA Mutation	p.Val554Asp(p.V554D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301608
Start	75973661:75973661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394A>G
AA Mutation	p.Ile132Val(p.I132V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301608
Start	75973768:75973768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287T>G
AA Mutation	p.Phe96Cys(p.F96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301608
Start	75955673:75955673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143260706
CDS Mutation	c.667G>A
AA Mutation	p.Val223Ile(p.V223I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301608
Start	75979054:75979054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20G>T
AA Mutation	p.Arg7Met(p.R7M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301608
Start	75953482:75953482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913G>A
AA Mutation	p.Ala305Thr(p.A305T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301608
Start	75949577:75949577(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1502delA
AA Mutation	p.Asn501ThrfsTer6(p.N501Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000301608
Start	75949215:75949215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1728+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ACOX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301608
Start	75953548:75953548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847T>A
AA Mutation	p.Ser283Thr(p.S283T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript