Colon Cancer: Gene >> MMP9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46012468:46012468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373663809
CDS Mutation	c.1216G>A
AA Mutation	p.Ala406Thr(p.A406T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46013672:46013672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1626C>A
AA Mutation	p.Phe542Leu(p.F542L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46013471:46013471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1547G>A
AA Mutation	p.Cys516Tyr(p.C516Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46016274:46016274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200118434
CDS Mutation	c.2030G>A
AA Mutation	p.Arg677His(p.R677H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46014165:46014165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1792C>A
AA Mutation	p.Pro598Thr(p.P598T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46010566:46010566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455C>T
AA Mutation	p.Thr152Met(p.T152M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46013261:46013261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337G>A
AA Mutation	p.Arg446His(p.R446H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46011687:46011687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937T>C
AA Mutation	p.Trp313Arg(p.W313R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46013309:46013309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1385C>T
AA Mutation	p.Thr462Met(p.T462M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46011286:46011286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793G>A
AA Mutation	p.Asp265Asn(p.D265N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46010049:46010049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322C>G
AA Mutation	p.Gln108Glu(p.Q108E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46016286:46016286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774687719
CDS Mutation	c.2042G>A
AA Mutation	p.Arg681His(p.R681H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46012238:46012238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099G>A
AA Mutation	p.Gly367Arg(p.G367R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46009009:46009009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83T>C
AA Mutation	p.Leu28Pro(p.L28P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46009992:46009992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265G>A
AA Mutation	p.Ala89Thr(p.A89T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46010969:46010969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568C>T
AA Mutation	p.His190Tyr(p.H190Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46013692:46013692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1646G>A
AA Mutation	p.Arg549Gln(p.R549Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46011702:46011702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776052269
CDS Mutation	c.952G>A
AA Mutation	p.Ala318Thr(p.A318T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372330
Start	46010956:46010956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763027034
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372330
Start	46012264:46012264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372330
Start	46008998:46008998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372330
Start	46013355:46013355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1431C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MMP9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46011281:46011281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788A>G
AA Mutation	p.Asp263Gly(p.D263G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46013321:46013321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397C>T
AA Mutation	p.Thr466Met(p.T466M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46010541:46010541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>A
AA Mutation	p.Ala144Thr(p.A144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372330
Start	46013777:46013777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731G>T
AA Mutation	p.Lys577Asn(p.K577N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372330
Start	46011013:46011013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000372330
Start	46013798:46013798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript