Colon Cancer: Gene >> MMP25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336577
Start	3050311:3050311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.426G>T
AA Mutation	p.Met142Ile(p.M142I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336577
Start	3058547:3058547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371274366
CDS Mutation	c.1295G>A
AA Mutation	p.Arg432His(p.R432H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336577
Start	3050436:3050436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551C>A
AA Mutation	p.Pro184His(p.P184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336577
Start	3057315:3057315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140235913
CDS Mutation	c.844G>A
AA Mutation	p.Ala282Thr(p.A282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336577
Start	3050089:3050089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200558581
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Cys(p.R105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336577
Start	3047483:3047483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168G>T
AA Mutation	p.Glu56Asp(p.E56D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336577
Start	3050515:3050515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146506930
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336577
Start	3057317:3057317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139849403
CDS Mutation	c.846G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336577
Start	3050374:3050374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336577
Start	3050088:3050088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143114141
CDS Mutation	c.312G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000336577
Start	3059077:3059077(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1673delG
AA Mutation	p.Gly558ValfsTer2(p.G558Vfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MMP25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336577
Start	3058873:3058873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1464G>T
AA Mutation	p.Lys488Asn(p.K488N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript