Colon Cancer: Gene >> MMP15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58041745:58041745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757069983
CDS Mutation	c.1039C>T
AA Mutation	p.Pro347Ser(p.P347S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58037607:58037607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199836131
CDS Mutation	c.298G>A
AA Mutation	p.Glu100Lys(p.E100K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58043571:58043571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1514G>T
AA Mutation	p.Ser505Ile(p.S505I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58040078:58040078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.644C>A
AA Mutation	p.Thr215Asn(p.T215N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58038327:58038327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373C>A
AA Mutation	p.Leu125Met(p.L125M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58041670:58041670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572888530
CDS Mutation	c.964C>T
AA Mutation	p.Arg322Trp(p.R322W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58039939:58039939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780493873
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Cys(p.R169C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58042333:58042333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1267T>C
AA Mutation	p.Tyr423His(p.Y423H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219271
Start	58042347:58042347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775288075
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219271
Start	58045047:58045047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200425285
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000219271
Start	58045398:58045398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147317164
CDS Mutation	c.1962G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MMP15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58040065:58040065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631C>T
AA Mutation	p.Pro211Ser(p.P211S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000219271
Start	58040665:58040665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148331048
CDS Mutation	c.877G>A
AA Mutation	p.Glu293Lys(p.E293K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript