Colon Cancer: Gene >> MMP17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360564
Start	131838692:131838692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144538442
CDS Mutation	c.373C>T
AA Mutation	p.Arg125Cys(p.R125C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360564
Start	131849954:131849954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374439053
CDS Mutation	c.1357C>T
AA Mutation	p.Arg453Cys(p.R453C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360564
Start	131841783:131841783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760432391
CDS Mutation	c.866G>A
AA Mutation	p.Arg289His(p.R289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360564
Start	131851106:131851106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1644A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360564
Start	131840687:131840687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762066684
CDS Mutation	c.537G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360564
Start	131840654:131840654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360564
Start	131840808:131840808(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.661delG
AA Mutation	p.Asp221ThrfsTer36(p.D221Tfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MMP17

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360564
Start	131844025:131844025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147967308
CDS Mutation	c.912G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360564
Start	131851073:131851073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762027563
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360564
Start	131849860:131849860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1263C>A
Mutation Classification	Silent
Feature Type	Transcript