Colon Cancer: Gene >> METAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323666
Start	95494100:95494100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473T>C
AA Mutation	p.Leu158Ser(p.L158S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323666
Start	95476142:95476142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.223G>A
AA Mutation	p.Ala75Thr(p.A75T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323666
Start	95494090:95494090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463A>C
AA Mutation	p.Lys155Gln(p.K155Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323666
Start	95504105:95504105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908C>T
AA Mutation	p.Ala303Val(p.A303V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323666
Start	95513835:95513835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112506052
CDS Mutation	c.1368G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323666
Start	95476078:95476078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323666
Start	95512823:95512823(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1093delA
AA Mutation	p.Thr365ProfsTer20(p.T365Pfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000323666
Start	95485953:95485953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>T
AA Mutation	p.Glu134Ter(p.E134*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000323666
Start	95511925:95511925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995C>A
AA Mutation	p.Ser332Ter(p.S332*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323666
Start	95476085:95476086(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.166_167insAGAAA
AA Mutation	p.Pro56GlnfsTer14(p.P56Qfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323666
Start	95476086:95476087(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.167_168insATTATTG
AA Mutation	p.Asp57LeufsTer3(p.D57Lfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> METAP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323666
Start	95476155:95476155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236A>C
AA Mutation	p.Lys79Thr(p.K79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323666
Start	95485913:95485913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360A>G
AA Mutation	p.Ile120Met(p.I120M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript