Colon Cancer: Gene >> METAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296411
Start	99043376:99043376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.644A>G
AA Mutation	p.Asp215Gly(p.D215G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296411
Start	99048811:99048811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866G>A
AA Mutation	p.Arg289Gln(p.R289Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296411
Start	99048793:99048793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848A>T
AA Mutation	p.Asn283Ile(p.N283I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296411
Start	99043269:99043269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296411
Start	99028914:99028915(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.162_163insCATTTTAAGGAATATT
AA Mutation	p.Ala55HisfsTer9(p.A55Hfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> METAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296411
Start	99034292:99034292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229C>A
AA Mutation	p.Pro77Thr(p.P77T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript