Colon Cancer: Gene >> MMP11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215743
Start	23779388:23779388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563846943
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Cys(p.R104C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215743
Start	23780498:23780498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143231653
CDS Mutation	c.478G>A
AA Mutation	p.Ala160Thr(p.A160T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215743
Start	23783425:23783425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348C>A
AA Mutation	p.Leu450Met(p.L450M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215743
Start	23781081:23781081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839A>G
AA Mutation	p.Asn280Ser(p.N280S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000215743
Start	23779344:23779344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266T>C
AA Mutation	p.Leu89Pro(p.L89P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000215743
Start	23782373:23782373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778551635
CDS Mutation	c.1223A>G
AA Mutation	p.Tyr408Cys(p.Y408C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215743
Start	23779327:23779327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144178537
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215743
Start	23781402:23781402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_lost
Transcription ID	ENST00000215743
Start	23783544:23783544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1467A>G
AA Mutation	p.Ter489TrpextTer10(p.*489Wext*10)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MMP11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215743
Start	23780649:23780649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550A>G
AA Mutation	p.Lys184Glu(p.K184E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215743
Start	23779328:23779328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376901794
CDS Mutation	c.250G>A
AA Mutation	p.Asp84Asn(p.D84N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215743
Start	23780678:23780678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369986636
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript