Colon Cancer: Gene >> MMP27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260229
Start	102695044:102695044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528734512
CDS Mutation	c.956C>T
AA Mutation	p.Ala319Val(p.A319V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260229
Start	102703110:102703110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350A>G
AA Mutation	p.Asn117Ser(p.N117S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260229
Start	102704574:102704574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304A>G
AA Mutation	p.Thr102Ala(p.T102A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260229
Start	102696752:102696752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703T>C
AA Mutation	p.Phe235Leu(p.F235L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260229
Start	102704668:102704668(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.210delT
AA Mutation	p.Phe70LeufsTer3(p.F70Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000260229
Start	102703046:102703046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>A
AA Mutation	p.Trp138Ter(p.W138*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MMP27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260229
Start	102691955:102691955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353G>T
AA Mutation	p.Lys451Asn(p.K451N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript