Colon Cancer: Gene >> MMP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000236826
Start	102721485:102721485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538C>A
AA Mutation	p.Leu180Ile(p.L180I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000236826
Start	102718533:102718533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.665C>A
AA Mutation	p.Ser222Tyr(p.S222Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000236826
Start	102721430:102721430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593C>T
AA Mutation	p.Ala198Val(p.A198V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000236826
Start	102715384:102715384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956C>A
AA Mutation	p.Ser319Tyr(p.S319Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000236826
Start	102718491:102718491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707A>C
AA Mutation	p.Tyr236Ser(p.Y236S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236826
Start	102718550:102718550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236826
Start	102718436:102718436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750688454
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236826
Start	102722599:102722599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770460574
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000236826
Start	102722566:102722566(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.210delT
AA Mutation	p.Phe70LeufsTer3(p.F70Lfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000236826
Start	102722574:102722574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780366606
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Ter(p.R68*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MMP8

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236826
Start	102715401:102715401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530920765
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript