Colon Cancer: Gene >> MMP12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000571244
Start	102871858:102871858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445T>G
AA Mutation	p.Phe149Val(p.F149V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000571244
Start	102863154:102863154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1359C>A
AA Mutation	p.Phe453Leu(p.F453L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000571244
Start	102871906:102871906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782297288
CDS Mutation	c.397G>A
AA Mutation	p.Ala133Thr(p.A133T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000571244
Start	102867950:102867950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183458117
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Cys(p.R249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000571244
Start	102872955:102872955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260T>G
AA Mutation	p.Met87Arg(p.M87R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000571244
Start	102872897:102872897(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs782219122
CDS Mutation	c.318delG
AA Mutation	p.Val108TyrfsTer18(p.V108Yfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000571244
Start	102873025:102873025(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.190delA
AA Mutation	p.Ile64SerfsTer10(p.I64Sfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000571244
Start	102865813:102865813(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1168delT
AA Mutation	p.Tyr390IlefsTer7(p.Y390Ifs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000571244
Start	102872896:102872897(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.318dupG
AA Mutation	p.Pro107AlafsTer14(p.P107Afs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MMP12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000571244
Start	102867373:102867373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202044860
CDS Mutation	c.808C>T
AA Mutation	p.Arg270Cys(p.R270C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript