Colon Cancer: Gene >> MMP24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35254731:35254731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770843975
CDS Mutation	c.794C>T
AA Mutation	p.Thr265Met(p.T265M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35254737:35254737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800G>A
AA Mutation	p.Gly267Glu(p.G267E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35251960:35251960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759744987
CDS Mutation	c.451C>T
AA Mutation	p.Arg151Trp(p.R151W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35271677:35271677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752150455
CDS Mutation	c.1442G>A
AA Mutation	p.Arg481His(p.R481H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35251961:35251961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369700691
CDS Mutation	c.452G>A
AA Mutation	p.Arg151Gln(p.R151Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35274350:35274350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1679G>A
AA Mutation	p.Arg560His(p.R560H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35246974:35246974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381T>A
AA Mutation	p.Asp127Glu(p.D127E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35274410:35274410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370896350
CDS Mutation	c.1739G>A
AA Mutation	p.Arg580Gln(p.R580Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246186
Start	35274474:35274474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1803C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246186
Start	35263876:35263876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752992245
CDS Mutation	c.903G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MMP24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35274455:35274455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1784A>G
AA Mutation	p.Asp595Gly(p.D595G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246186
Start	35254701:35254701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764A>G
AA Mutation	p.Asp255Gly(p.D255G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript