Colon Cancer: Gene >> MMP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299855
Start	102842748:102842748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274T>C
AA Mutation	p.Cys92Arg(p.C92R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299855
Start	102840492:102840492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727C>T
AA Mutation	p.Leu243Phe(p.L243F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299855
Start	102836213:102836213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1347C>A
AA Mutation	p.Phe449Leu(p.F449L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299855
Start	102839195:102839195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984G>T
AA Mutation	p.Leu328Phe(p.L328F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299855
Start	102839179:102839179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000C>T
AA Mutation	p.Pro334Ser(p.P334S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299855
Start	102836171:102836171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1389G>T
AA Mutation	p.Lys463Asn(p.K463N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299855
Start	102840191:102840191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299855
Start	102843514:102843514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113324830
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299855
Start	102840550:102840550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375553123
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299855
Start	102842832:102842832(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.190delA
AA Mutation	p.Ile64SerfsTer12(p.I64Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000299855
Start	102842829:102842829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143174783
CDS Mutation	c.193C>T
AA Mutation	p.Arg65Ter(p.R65*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000299855
Start	102838549:102838549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1229+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MMP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299855
Start	102838700:102838700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080C>A
AA Mutation	p.Phe360Leu(p.F360L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299855
Start	102838656:102838656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124G>A
AA Mutation	p.Gly375Asp(p.G375D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript