Colon Cancer: Gene >> ACOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302819
Start	58526481:58526481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1331A>G
AA Mutation	p.Tyr444Cys(p.Y444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302819
Start	58530479:58530479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138459863
CDS Mutation	c.979C>T
AA Mutation	p.Arg327Trp(p.R327W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302819
Start	58534130:58534130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339C>A
AA Mutation	p.Asp113Glu(p.D113E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302819
Start	58524549:58524549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1403G>T
AA Mutation	p.Arg468Ile(p.R468I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302819
Start	58517315:58517315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1741A>G
AA Mutation	p.Ile581Val(p.I581V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302819
Start	58534963:58534963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302819
Start	58508983:58508983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1893T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302819
Start	58524479:58524479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302819
Start	58524538:58524539(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1413_1414delTC
AA Mutation	p.Pro472IlefsTer9(p.P472Ifs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302819
Start	58531721:58531721(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.675delG
AA Mutation	p.Ser226ValfsTer32(p.S226Vfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ACOX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302819
Start	58533492:58533492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536T>A
AA Mutation	p.Val179Glu(p.V179E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302819
Start	58531275:58531275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795G>A
Mutation Classification	Silent
Feature Type	Transcript