Colon Cancer: Gene >> MMP28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000605424
Start	35766816:35766816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1247G>A
AA Mutation	p.Arg416His(p.R416H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000605424
Start	35768367:35768367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.863G>A
AA Mutation	p.Gly288Glu(p.G288E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000605424
Start	35770222:35770222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.695G>A
AA Mutation	p.Arg232His(p.R232H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000605424
Start	35767778:35767778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142A>C
AA Mutation	p.Asn381Thr(p.N381T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605424
Start	35773331:35773331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605424
Start	35770140:35770140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.777G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605424
Start	35779072:35779072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184976878
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605424
Start	35778991:35778991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605424
Start	35766550:35766550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000605424
Start	35766803:35766803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000605424
Start	35766729:35766729(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1334delG
AA Mutation	p.Gly445AspfsTer107(p.G445Dfs*107)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MMP28

No Mutation Annotation!