Colon Cancer: Gene >> MMP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315274
Start	102791451:102791451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078T>C
AA Mutation	p.Tyr360His(p.Y360H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315274
Start	102795592:102795592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641G>A
AA Mutation	p.Arg214His(p.R214H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315274
Start	102791423:102791423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1106G>A
AA Mutation	p.Gly369Asp(p.G369D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315274
Start	102791382:102791382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147G>A
AA Mutation	p.Glu383Lys(p.E383K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315274
Start	102792641:102792641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778882706
CDS Mutation	c.997G>A
AA Mutation	p.Glu333Lys(p.E333K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315274
Start	102797371:102797371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235C>T
AA Mutation	p.Pro79Ser(p.P79S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315274
Start	102797029:102797029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484T>C
AA Mutation	p.Ser162Pro(p.S162P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315274
Start	102798087:102798087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315274
Start	102792708:102792708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571363149
CDS Mutation	c.930G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MMP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315274
Start	102790484:102790484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1338A>C
AA Mutation	p.Lys446Asn(p.K446N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315274
Start	102790710:102790710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1293G>T
AA Mutation	p.Met431Ile(p.M431I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315274
Start	102797396:102797396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210C>T
Mutation Classification	Silent
Feature Type	Transcript